ENST00000367698.4:c.1265T>C
MANE Select
|
ENSP00000356671.3:p.Ile422Thr
|
|
ENST00000367698.3:c.1265T>C
|
ENSP00000356671.3:p.Ile422Thr
|
|
ENST00000617423.4:c.650T>C
|
ENSP00000478688.1:p.Ile217Thr
|
|
NM_000488.3:c.1265T>C , LRG_577t1:c.1265T>C
|
NP_000479.1:p.Ile422Thr
|
|
XM_005245198.2:c.1121T>C
|
XP_005245255.1:p.Ile374Thr
|
|
NM_001365052.1:c.1121T>C
|
NP_001351981.1:p.Ile374Thr
|
|
NM_000488.4:c.1265T>C
MANE Select
|
NP_000479.1:p.Ile422Thr
|
|
NM_001365052.2:c.1121T>C
|
NP_001351981.1:p.Ile374Thr
|
|
NM_001386302.1:c.1388T>C
|
NP_001373231.1:p.Ile463Thr
|
|
NM_001386303.1:c.1346T>C
|
NP_001373232.1:p.Ile449Thr
|
|
NM_001386304.1:c.1244T>C
|
NP_001373233.1:p.Ile415Thr
|
|
NM_001386305.1:c.1208T>C
|
NP_001373234.1:p.Ile403Thr
|
|
NM_001386306.1:c.1049T>C
|
NP_001373235.1:p.Ile350Thr
|
|