ENST00000367698.4:c.1374A>C
MANE Select
|
ENSP00000356671.3:p.Val458=
|
|
ENST00000367698.3:c.1374A>C
|
ENSP00000356671.3:p.Val458=
|
|
ENST00000617423.4:c.759A>C
|
ENSP00000478688.1:p.Val253=
|
|
NM_000488.3:c.1374A>C , LRG_577t1:c.1374A>C
|
NP_000479.1:p.Val458=
|
|
XM_005245198.2:c.1230A>C
|
XP_005245255.1:p.Val410=
|
|
NM_001365052.1:c.1230A>C
|
NP_001351981.1:p.Val410=
|
|
NM_000488.4:c.1374A>C
MANE Select
|
NP_000479.1:p.Val458=
|
|
NM_001365052.2:c.1230A>C
|
NP_001351981.1:p.Val410=
|
|
NM_001386302.1:c.1497A>C
|
NP_001373231.1:p.Val499=
|
|
NM_001386303.1:c.1455A>C
|
NP_001373232.1:p.Val485=
|
|
NM_001386304.1:c.1353A>C
|
NP_001373233.1:p.Val451=
|
|
NM_001386305.1:c.1317A>C
|
NP_001373234.1:p.Val439=
|
|
NM_001386306.1:c.1158A>C
|
NP_001373235.1:p.Val386=
|
|