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ENST00000356839.10:c.796C=
MANE Select
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ENSP00000349297.5:p.Pro266=
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|
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ENST00000322910.9:c.*751C=
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ENSP00000325395.5:n.*751C=
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ENST00000350303.9:c.730C=
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ENSP00000344152.5:p.Pro244=
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ENST00000356839.9:c.796C=
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ENSP00000349297.5:p.Pro266=
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ENST00000543245.6:c.865C=
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ENSP00000438689.2:p.Pro289=
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ENST00000577191.5:n.968C=
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ENST00000581378.5:c.514C=
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ENST00000582379.1:n.180C=
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NM_000018.3:c.796C=
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NP_000009.1:p.Pro266=
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NM_001033859.2:c.730C=
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NP_001029031.1:p.Pro244=
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NM_001270447.1:c.865C=
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NP_001257376.1:p.Pro289=
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NM_001270448.1:c.568C=
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NP_001257377.1:p.Pro190=
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XM_006721516.2:c.796C=
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XP_006721579.2:p.Pro266=
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XM_011523829.1:c.796C=
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XP_011522131.1:p.Pro266=
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|
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XM_011523830.1:c.796C=
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XP_011522132.1:p.Pro266=
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XR_934021.1:n.903C=
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XR_934022.1:n.903C=
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XR_934023.1:n.903C=
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|
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XM_006721516.3:c.796C=
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XP_006721579.2:p.Pro266=
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XM_011523829.2:c.796C=
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XP_011522131.1:p.Pro266=
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|
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XM_011523830.2:c.796C=
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XP_011522132.1:p.Pro266=
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|
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XM_024450741.1:c.796C=
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XP_024306509.1:p.Pro266=
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XR_934021.2:n.855C=
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|
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XR_934022.2:n.855C=
|
|
|
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XR_934023.2:n.855C=
|
|
|
|
NM_000018.4:c.796C=
MANE Select
|
NP_000009.1:p.Pro266=
|
|
|
NM_001033859.3:c.730C=
|
NP_001029031.1:p.Pro244=
|
|
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NM_001270447.2:c.865C=
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NP_001257376.1:p.Pro289=
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|
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NM_001270448.2:c.568C=
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NP_001257377.1:p.Pro190=
|
|
