ENST00000286355.10:c.3532C>G
MANE Select
|
ENSP00000286355.5:p.Pro1178Ala
|
|
ENST00000286355.9:c.3532C>G
|
ENSP00000286355.5:p.Pro1178Ala
|
|
ENST00000377928.7:c.3139C>G
|
ENSP00000367161.3:p.Pro1047Ala
|
|
NM_001115.2:c.3532C>G
|
NP_001106.1:p.Pro1178Ala
|
|
XM_005250769.2:c.3442C>G
|
XP_005250826.1:p.Pro1148Ala
|
|
XM_006716501.2:c.3334C>G
|
XP_006716564.1:p.Pro1112Ala
|
|
XM_005250769.3:c.3442C>G
|
XP_005250826.1:p.Pro1148Ala
|
|
XM_006716501.3:c.3334C>G
|
XP_006716564.1:p.Pro1112Ala
|
|
XM_017013006.1:c.3244C>G
|
XP_016868495.1:p.Pro1082Ala
|
|
NM_001115.3:c.3532C>G
MANE Select
|
NP_001106.1:p.Pro1178Ala
|
|