ENST00000367698.4:c.1381C>A
MANE Select
|
ENSP00000356671.3:p.Pro461Thr
|
|
ENST00000367698.3:c.1381C>A
|
ENSP00000356671.3:p.Pro461Thr
|
|
ENST00000617423.4:c.766C>A
|
ENSP00000478688.1:p.Pro256Thr
|
|
NM_000488.3:c.1381C>A , LRG_577t1:c.1381C>A
|
NP_000479.1:p.Pro461Thr
|
|
XM_005245198.2:c.1237C>A
|
XP_005245255.1:p.Pro413Thr
|
|
NM_001365052.1:c.1237C>A
|
NP_001351981.1:p.Pro413Thr
|
|
NM_000488.4:c.1381C>A
MANE Select
|
NP_000479.1:p.Pro461Thr
|
|
NM_001365052.2:c.1237C>A
|
NP_001351981.1:p.Pro413Thr
|
|
NM_001386302.1:c.1504C>A
|
NP_001373231.1:p.Pro502Thr
|
|
NM_001386303.1:c.1462C>A
|
NP_001373232.1:p.Pro488Thr
|
|
NM_001386304.1:c.1360C>A
|
NP_001373233.1:p.Pro454Thr
|
|
NM_001386305.1:c.1324C>A
|
NP_001373234.1:p.Pro442Thr
|
|
NM_001386306.1:c.1165C>A
|
NP_001373235.1:p.Pro389Thr
|
|