ENST00000317961.9:c.3649T>G
MANE Select
|
ENSP00000322408.4:p.Ser1217Ala
|
|
ENST00000317961.8:c.3649T>G
|
ENSP00000322408.4:p.Ser1217Ala
|
|
ENST00000382806.6:c.3478T>G
|
ENSP00000372256.2:p.Ser1160Ala
|
|
ENST00000415360.1:c.565T>G
|
ENSP00000389433.1:p.Ser189Ala
|
|
ENST00000440077.5:c.3526T>G
|
ENSP00000398543.1:p.Ser1176Ala
|
|
ENST00000469599.6:n.2247T>G
|
|
|
ENST00000492117.1:n.3541T>G
|
|
|
ENST00000541639.5:c.3742T>G
|
ENSP00000444293.1:p.Ser1248Ala
|
|
NM_001146705.1:c.3742T>G
|
NP_001140177.1:p.Ser1248Ala
|
|
NM_001146706.1:c.3478T>G
|
NP_001140178.1:p.Ser1160Ala
|
|
NM_004653.4:c.3649T>G
|
NP_004644.2:p.Ser1217Ala
|
|
XM_005262560.1:c.3514T>G
|
XP_005262617.1:p.Ser1172Ala
|
|
XM_005262561.1:c.3418T>G
|
XP_005262618.1:p.Ser1140Ala
|
|
XM_011531468.1:c.3571T>G
|
XP_011529770.1:p.Ser1191Ala
|
|
XR_244571.2:n.3937T>G
|
|
|
XR_430568.2:n.4271T>G
|
|
|
XM_005262560.3:c.3514T>G
|
XP_005262617.1:p.Ser1172Ala
|
|
XM_005262561.3:c.3418T>G
|
XP_005262618.1:p.Ser1140Ala
|
|
XM_011531468.3:c.3571T>G
|
XP_011529770.1:p.Ser1191Ala
|
|
XM_024452495.1:c.1639T>G
|
XP_024308263.1:p.Ser547Ala
|
|
XM_024452496.1:c.1405T>G
|
XP_024308264.1:p.Ser469Ala
|
|
XR_001756009.2:n.4387T>G
|
|
|
XR_001756010.2:n.4387T>G
|
|
|
XR_001756011.2:n.4252T>G
|
|
|
XR_001756012.2:n.4400T>G
|
|
|
XR_001756013.2:n.3718T>G
|
|
|
XR_002958832.1:n.3819T>G
|
|
|
XR_002958834.1:n.4043T>G
|
|
|
XR_002958835.1:n.3926T>G
|
|
|
XR_002958836.1:n.4609T>G
|
|
|
XR_002958837.1:n.4416T>G
|
|
|
XR_244571.4:n.3936T>G
|
|
|
XR_430568.4:n.4270T>G
|
|
|
NM_001146706.2:c.3478T>G
|
NP_001140178.1:p.Ser1160Ala
|
|
NM_004653.5:c.3649T>G
MANE Select
|
NP_004644.2:p.Ser1217Ala
|
|
NM_001146705.2:c.3742T>G
|
NP_001140177.1:p.Ser1248Ala
|
|