ENST00000303941.4:c.1222C>G
MANE Select
|
ENSP00000306678.3:p.Pro408Ala
|
|
ENST00000303941.3:c.1222C>G
|
ENSP00000306678.3:p.Pro408Ala
|
|
NM_178510.1:c.1222C>G
|
NP_848605.1:p.Pro408Ala
|
|
XM_011542736.1:c.1255C>G
|
XP_011541038.1:p.Pro419Ala
|
|
XM_011542737.1:c.1225C>G
|
XP_011541039.1:p.Pro409Ala
|
|
XM_011542738.1:c.1033C>G
|
XP_011541040.1:p.Pro345Ala
|
|
XM_011542736.2:c.1255C>G
|
XP_011541038.1:p.Pro419Ala
|
|
XM_011542737.2:c.1225C>G
|
XP_011541039.1:p.Pro409Ala
|
|
XM_011542738.2:c.1033C>G
|
XP_011541040.1:p.Pro345Ala
|
|
XM_017017475.1:c.1252C>G
|
XP_016872964.1:p.Pro418Ala
|
|
NM_178510.2:c.1222C>G
MANE Select
|
NP_848605.1:p.Pro408Ala
|
|