ENST00000367698.4:c.1262T>A
MANE Select
|
ENSP00000356671.3:p.Val421Glu
|
|
ENST00000367698.3:c.1262T>A
|
ENSP00000356671.3:p.Val421Glu
|
|
ENST00000617423.4:c.647T>A
|
ENSP00000478688.1:p.Val216Glu
|
|
NM_000488.3:c.1262T>A , LRG_577t1:c.1262T>A
|
NP_000479.1:p.Val421Glu
|
|
XM_005245198.2:c.1118T>A
|
XP_005245255.1:p.Val373Glu
|
|
NM_001365052.1:c.1118T>A
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NP_001351981.1:p.Val373Glu
|
|
NM_000488.4:c.1262T>A
MANE Select
|
NP_000479.1:p.Val421Glu
|
|
NM_001365052.2:c.1118T>A
|
NP_001351981.1:p.Val373Glu
|
|
NM_001386302.1:c.1385T>A
|
NP_001373231.1:p.Val462Glu
|
|
NM_001386303.1:c.1343T>A
|
NP_001373232.1:p.Val448Glu
|
|
NM_001386304.1:c.1241T>A
|
NP_001373233.1:p.Val414Glu
|
|
NM_001386305.1:c.1205T>A
|
NP_001373234.1:p.Val402Glu
|
|
NM_001386306.1:c.1046T>A
|
NP_001373235.1:p.Val349Glu
|
|