ENST00000317961.9:c.3610C>G
MANE Select
|
ENSP00000322408.4:p.Pro1204Ala
|
|
ENST00000317961.8:c.3610C>G
|
ENSP00000322408.4:p.Pro1204Ala
|
|
ENST00000382806.6:c.3439C>G
|
ENSP00000372256.2:p.Pro1147Ala
|
|
ENST00000415360.1:c.526C>G
|
ENSP00000389433.1:p.Pro176Ala
|
|
ENST00000440077.5:c.3487C>G
|
ENSP00000398543.1:p.Pro1163Ala
|
|
ENST00000469599.6:n.2208C>G
|
|
|
ENST00000492117.1:n.3502C>G
|
|
|
ENST00000541639.5:c.3703C>G
|
ENSP00000444293.1:p.Pro1235Ala
|
|
NM_001146705.1:c.3703C>G
|
NP_001140177.1:p.Pro1235Ala
|
|
NM_001146706.1:c.3439C>G
|
NP_001140178.1:p.Pro1147Ala
|
|
NM_004653.4:c.3610C>G
|
NP_004644.2:p.Pro1204Ala
|
|
XM_005262560.1:c.3475C>G
|
XP_005262617.1:p.Pro1159Ala
|
|
XM_005262561.1:c.3379C>G
|
XP_005262618.1:p.Pro1127Ala
|
|
XM_011531468.1:c.3532C>G
|
XP_011529770.1:p.Pro1178Ala
|
|
XR_244571.2:n.3898C>G
|
|
|
XR_430568.2:n.4232C>G
|
|
|
XM_005262560.3:c.3475C>G
|
XP_005262617.1:p.Pro1159Ala
|
|
XM_005262561.3:c.3379C>G
|
XP_005262618.1:p.Pro1127Ala
|
|
XM_011531468.3:c.3532C>G
|
XP_011529770.1:p.Pro1178Ala
|
|
XM_024452495.1:c.1600C>G
|
XP_024308263.1:p.Pro534Ala
|
|
XM_024452496.1:c.1366C>G
|
XP_024308264.1:p.Pro456Ala
|
|
XR_001756009.2:n.4348C>G
|
|
|
XR_001756010.2:n.4348C>G
|
|
|
XR_001756011.2:n.4213C>G
|
|
|
XR_001756012.2:n.4361C>G
|
|
|
XR_001756013.2:n.3679C>G
|
|
|
XR_002958832.1:n.3780C>G
|
|
|
XR_002958834.1:n.4004C>G
|
|
|
XR_002958835.1:n.3887C>G
|
|
|
XR_002958836.1:n.4570C>G
|
|
|
XR_002958837.1:n.4377C>G
|
|
|
XR_244571.4:n.3897C>G
|
|
|
XR_430568.4:n.4231C>G
|
|
|
NM_001146706.2:c.3439C>G
|
NP_001140178.1:p.Pro1147Ala
|
|
NM_004653.5:c.3610C>G
MANE Select
|
NP_004644.2:p.Pro1204Ala
|
|
NM_001146705.2:c.3703C>G
|
NP_001140177.1:p.Pro1235Ala
|
|