ENST00000356839.10:c.625G>T
MANE Select
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ENSP00000349297.5:p.Glu209Ter
|
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ENST00000322910.9:c.*580G>T
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ENSP00000325395.5:n.*580G>T
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|
ENST00000350303.9:c.559G>T
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ENSP00000344152.5:p.Glu187Ter
|
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ENST00000356839.9:c.625G>T
|
ENSP00000349297.5:p.Glu209Ter
|
|
ENST00000543245.6:c.694G>T
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ENSP00000438689.2:p.Glu232Ter
|
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ENST00000577191.5:n.702G>T
|
|
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ENST00000577857.5:n.441G>T
|
|
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ENST00000579286.5:n.806G>T
|
|
|
ENST00000579886.2:c.463G>T
|
ENSP00000463246.1:p.Glu155Ter
|
|
ENST00000580365.1:n.356G>T
|
|
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ENST00000581378.5:c.343G>T
|
|
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ENST00000581562.5:n.527G>T
|
|
|
ENST00000582379.1:n.9G>T
|
|
|
ENST00000583312.5:c.640G>T
|
ENSP00000467920.1:p.Glu214Ter
|
|
ENST00000583760.1:n.407G>T
|
|
|
NM_000018.3:c.625G>T
|
NP_000009.1:p.Glu209Ter
|
|
NM_001033859.2:c.559G>T
|
NP_001029031.1:p.Glu187Ter
|
|
NM_001270447.1:c.694G>T
|
NP_001257376.1:p.Glu232Ter
|
|
NM_001270448.1:c.397G>T
|
NP_001257377.1:p.Glu133Ter
|
|
XM_006721516.2:c.625G>T
|
XP_006721579.2:p.Glu209Ter
|
|
XM_011523829.1:c.625G>T
|
XP_011522131.1:p.Glu209Ter
|
|
XM_011523830.1:c.625G>T
|
XP_011522132.1:p.Glu209Ter
|
|
XR_934021.1:n.732G>T
|
|
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XR_934022.1:n.732G>T
|
|
|
XR_934023.1:n.732G>T
|
|
|
XM_006721516.3:c.625G>T
|
XP_006721579.2:p.Glu209Ter
|
|
XM_011523829.2:c.625G>T
|
XP_011522131.1:p.Glu209Ter
|
|
XM_011523830.2:c.625G>T
|
XP_011522132.1:p.Glu209Ter
|
|
XM_024450741.1:c.625G>T
|
XP_024306509.1:p.Glu209Ter
|
|
XR_934021.2:n.684G>T
|
|
|
XR_934022.2:n.684G>T
|
|
|
XR_934023.2:n.684G>T
|
|
|
NM_000018.4:c.625G>T
MANE Select
|
NP_000009.1:p.Glu209Ter
|
|
NM_001033859.3:c.559G>T
|
NP_001029031.1:p.Glu187Ter
|
|
NM_001270447.2:c.694G>T
|
NP_001257376.1:p.Glu232Ter
|
|
NM_001270448.2:c.397G>T
|
NP_001257377.1:p.Glu133Ter
|
|