ENST00000362061.4:c.2836G>T
MANE Select
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ENSP00000355192.3:p.Gly946Cys
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ENST00000679417.1:c.*1999G>T
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ENSP00000506706.1:n.*1999G>T
|
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ENST00000680059.1:c.*354G>T
|
ENSP00000504944.1:n.*354G>T
|
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ENST00000681078.1:c.2836G>T
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ENSP00000506645.1:p.Gly946Cys
|
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ENST00000681190.1:c.2836G>T
|
ENSP00000506428.1:p.Gly946Cys
|
|
ENST00000681874.1:c.2776G>T
|
ENSP00000505162.1:p.Gly926Cys
|
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ENST00000362061.3:c.2836G>T
|
ENSP00000355192.3:p.Gly946Cys
|
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ENST00000367338.7:c.2836G>T
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ENSP00000356307.3:p.Gly946Cys
|
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NM_000069.2:c.2836G>T
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NP_000060.2:p.Gly946Cys
|
|
XM_005245478.2:c.2836G>T
|
XP_005245535.1:p.Gly946Cys
|
|
XM_005245478.3:c.2836G>T
|
XP_005245535.1:p.Gly946Cys
|
|
NM_000069.3:c.2836G>T
MANE Select
|
NP_000060.2:p.Gly946Cys
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