ENST00000356839.10:c.595G>T
MANE Select
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ENSP00000349297.5:p.Glu199Ter
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ENST00000322910.9:c.*550G>T
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ENSP00000325395.5:n.*550G>T
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ENST00000350303.9:c.529G>T
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ENSP00000344152.5:p.Glu177Ter
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ENST00000356839.9:c.595G>T
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ENSP00000349297.5:p.Glu199Ter
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ENST00000543245.6:c.664G>T
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ENSP00000438689.2:p.Glu222Ter
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ENST00000577191.5:n.672G>T
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|
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ENST00000577433.5:n.803G>T
|
|
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ENST00000577857.5:n.411G>T
|
|
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ENST00000579286.5:n.776G>T
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|
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ENST00000579886.2:c.433G>T
|
ENSP00000463246.1:p.Glu145Ter
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ENST00000580365.1:n.326G>T
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|
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ENST00000581378.5:c.313G>T
|
|
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ENST00000581562.5:n.525-297G>T
|
|
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ENST00000583312.5:c.595G>T
|
ENSP00000467920.1:p.Glu199Ter
|
|
ENST00000583760.1:n.377G>T
|
|
|
NM_000018.3:c.595G>T
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NP_000009.1:p.Glu199Ter
|
|
NM_001033859.2:c.529G>T
|
NP_001029031.1:p.Glu177Ter
|
|
NM_001270447.1:c.664G>T
|
NP_001257376.1:p.Glu222Ter
|
|
NM_001270448.1:c.367G>T
|
NP_001257377.1:p.Glu123Ter
|
|
XM_006721516.2:c.595G>T
|
XP_006721579.2:p.Glu199Ter
|
|
XM_011523829.1:c.595G>T
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XP_011522131.1:p.Glu199Ter
|
|
XM_011523830.1:c.595G>T
|
XP_011522132.1:p.Glu199Ter
|
|
XR_934021.1:n.702G>T
|
|
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XR_934022.1:n.702G>T
|
|
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XR_934023.1:n.702G>T
|
|
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XM_006721516.3:c.595G>T
|
XP_006721579.2:p.Glu199Ter
|
|
XM_011523829.2:c.595G>T
|
XP_011522131.1:p.Glu199Ter
|
|
XM_011523830.2:c.595G>T
|
XP_011522132.1:p.Glu199Ter
|
|
XM_024450741.1:c.595G>T
|
XP_024306509.1:p.Glu199Ter
|
|
XR_934021.2:n.654G>T
|
|
|
XR_934022.2:n.654G>T
|
|
|
XR_934023.2:n.654G>T
|
|
|
NM_000018.4:c.595G>T
MANE Select
|
NP_000009.1:p.Glu199Ter
|
|
NM_001033859.3:c.529G>T
|
NP_001029031.1:p.Glu177Ter
|
|
NM_001270447.2:c.664G>T
|
NP_001257376.1:p.Glu222Ter
|
|
NM_001270448.2:c.367G>T
|
NP_001257377.1:p.Glu123Ter
|
|