|
ENST00000617875.6:c.3313G>A
MANE Select
|
ENSP00000482313.2:p.Gly1105Ser
|
|
|
ENST00000301323.7:c.330G>A
|
|
|
|
ENST00000529424.2:n.50-202G>A
|
|
|
|
ENST00000531875.2:c.559G>A
|
ENSP00000477910.1:p.Gly187Ser
|
|
|
ENST00000617875.4:c.3313G>A
|
ENSP00000482313.1:p.Gly1105Ser
|
|
|
ENST00000621189.4:c.2242G>A
|
ENSP00000483145.1:p.Gly748Ser
|
|
|
NM_004260.3:c.3313G>A
|
NP_004251.3:p.Gly1105Ser
|
|
|
XM_011517380.1:c.3388G>A
|
XP_011515682.1:p.Gly1130Ser
|
|
|
XM_011517381.1:c.3292G>A
|
XP_011515683.1:p.Gly1098Ser
|
|
|
XM_011517382.1:c.3196G>A
|
XP_011515684.1:p.Gly1066Ser
|
|
|
XM_011517383.1:c.3190G>A
|
XP_011515685.1:p.Gly1064Ser
|
|
|
XM_011517384.1:c.3115G>A
|
XP_011515686.1:p.Gly1039Ser
|
|
|
XM_011517385.1:c.2251G>A
|
XP_011515687.1:p.Gly751Ser
|
|
|
XR_928366.1:n.3352+153G>A
|
|
|
|
XR_928367.1:n.3368G>A
|
|
|
|
XR_928368.1:n.3261G>A
|
|
|
|
XM_011517384.3:c.3115G>A
|
XP_011515686.1:p.Gly1039Ser
|
|
|
XM_017013991.2:c.3478G>A
|
XP_016869480.1:p.Gly1160Ser
|
|
|
XM_017013992.2:c.3403G>A
|
XP_016869481.1:p.Gly1135Ser
|
|
|
XM_017013993.2:c.3388G>A
|
XP_016869482.1:p.Gly1130Ser
|
|
|
XM_017013994.2:c.3382G>A
|
XP_016869483.1:p.Gly1128Ser
|
|
|
XM_017013995.2:c.3313G>A
|
XP_016869484.1:p.Gly1105Ser
|
|
|
XM_017013996.2:c.3478G>A
|
XP_016869485.1:p.Gly1160Ser
|
|
|
XM_017013997.2:c.3280G>A
|
XP_016869486.1:p.Gly1094Ser
|
|
|
XM_017013998.1:c.3403G>A
|
XP_016869487.1:p.Gly1135Ser
|
|
|
XM_017013999.2:c.3190G>A
|
XP_016869488.1:p.Gly1064Ser
|
|
|
XM_017014000.1:c.2341G>A
|
XP_016869489.1:p.Gly781Ser
|
|
|
XM_017014001.2:c.2251G>A
|
XP_016869490.1:p.Gly751Ser
|
|
|
XR_001745626.2:n.3438+153G>A
|
|
|
|
XR_001745627.2:n.3454G>A
|
|
|
|
XR_001745628.2:n.3345G>A
|
|
|
|
XR_001745629.2:n.3208G>A
|
|
|
|
XR_001745630.2:n.3010G>A
|
|
|
|
NM_004260.4:c.3313G>A
MANE Select
|
NP_004251.4:p.Gly1105Ser
|
|
