ENST00000576204.6:n.891G>A
|
|
|
ENST00000622290.5:c.*200G>A
|
ENSP00000483331.2:n.*200G>A
|
|
ENST00000205557.12:c.4028G>A
MANE Select
|
ENSP00000205557.7:p.Ser1343Asn
|
|
ENST00000640696.1:c.842G>A
|
ENSP00000492197.1:p.Ser281Asn
|
|
ENST00000205557.11:c.4028G>A
|
ENSP00000205557.7:p.Ser1343Asn
|
|
ENST00000456970.6:c.3653G>A
|
ENSP00000405002.2:n.3653G>A
|
|
ENST00000576204.5:n.891G>A
|
|
|
ENST00000622290.4:c.*1237G>A
|
ENSP00000483331.1:n.*1237G>A
|
|
NM_001171.5:c.4028G>A
|
NP_001162.4:p.Ser1343Asn
|
|
XM_011522479.1:c.3995G>A
|
XP_011520781.1:p.Ser1332Asn
|
|
XM_011522480.1:c.3686G>A
|
XP_011520782.1:p.Ser1229Asn
|
|
XM_011522481.1:c.3686G>A
|
XP_011520783.1:p.Ser1229Asn
|
|
XR_933134.1:n.539-4895C>T
|
|
|
NM_001351800.1:c.3686G>A
|
NP_001338729.1:p.Ser1229Asn
|
|
NR_147784.1:n.3690G>A
|
|
|
XM_011522479.2:c.3995G>A
|
XP_011520781.1:p.Ser1332Asn
|
|
XM_011522481.3:c.3686G>A
|
XP_011520783.1:p.Ser1229Asn
|
|
XM_017023212.1:c.3860G>A
|
XP_016878701.1:p.Ser1287Asn
|
|
XM_024450261.1:c.4064G>A
|
XP_024306029.1:p.Ser1355Asn
|
|
NM_001171.6:c.4028G>A
MANE Select
|
NP_001162.5:p.Ser1343Asn
|
|