ENST00000367698.4:c.1381C>G
MANE Select
|
ENSP00000356671.3:p.Pro461Ala
|
|
ENST00000367698.3:c.1381C>G
|
ENSP00000356671.3:p.Pro461Ala
|
|
ENST00000617423.4:c.766C>G
|
ENSP00000478688.1:p.Pro256Ala
|
|
NM_000488.3:c.1381C>G , LRG_577t1:c.1381C>G
|
NP_000479.1:p.Pro461Ala
|
|
XM_005245198.2:c.1237C>G
|
XP_005245255.1:p.Pro413Ala
|
|
NM_001365052.1:c.1237C>G
|
NP_001351981.1:p.Pro413Ala
|
|
NM_000488.4:c.1381C>G
MANE Select
|
NP_000479.1:p.Pro461Ala
|
|
NM_001365052.2:c.1237C>G
|
NP_001351981.1:p.Pro413Ala
|
|
NM_001386302.1:c.1504C>G
|
NP_001373231.1:p.Pro502Ala
|
|
NM_001386303.1:c.1462C>G
|
NP_001373232.1:p.Pro488Ala
|
|
NM_001386304.1:c.1360C>G
|
NP_001373233.1:p.Pro454Ala
|
|
NM_001386305.1:c.1324C>G
|
NP_001373234.1:p.Pro442Ala
|
|
NM_001386306.1:c.1165C>G
|
NP_001373235.1:p.Pro389Ala
|
|