ENST00000360319.9:c.2356G>T
|
ENSP00000353467.4:p.Ala786Ser
|
|
ENST00000369850.10:c.2356G>T
MANE Select
|
ENSP00000358866.3:p.Ala786Ser
|
|
ENST00000369856.8:c.2275G>T
|
ENSP00000358872.4:p.Ala759Ser
|
|
ENST00000422373.6:c.2356G>T
|
ENSP00000416926.2:p.Ala786Ser
|
|
ENST00000610817.5:c.2413G>T
|
ENSP00000480593.2:n.2413G>T
|
|
ENST00000673639.2:c.279+2727G>T
|
|
|
ENST00000676696.1:c.2635G>T
|
ENSP00000503392.1:n.2635G>T
|
|
ENST00000344736.8:c.2356G>T
|
ENSP00000358863.3:p.Ala786Ser
|
|
ENST00000360319.8:c.2356G>T
|
ENSP00000353467.4:p.Ala786Ser
|
|
ENST00000369850.7:c.2356G>T
|
ENSP00000358866.3:p.Ala786Ser
|
|
ENST00000369856.7:c.2275G>T
|
ENSP00000358872.4:p.Ala759Ser
|
|
ENST00000420627.5:c.2312G>T
|
ENSP00000408921.1:n.2312G>T
|
|
ENST00000422373.5:c.2356G>T
|
ENSP00000416926.1:p.Ala786Ser
|
|
ENST00000610817.4:c.2275G>T
|
ENSP00000480593.1:p.Ala759Ser
|
|
NM_001110556.1:c.2356G>T
|
NP_001104026.1:p.Ala786Ser
|
|
NM_001456.3:c.2356G>T
|
NP_001447.2:p.Ala786Ser
|
|
XM_011531127.1:c.2356G>T
|
XP_011529429.1:p.Ala786Ser
|
|
XM_011531128.1:c.2356G>T
|
XP_011529430.1:p.Ala786Ser
|
|
XM_011531129.1:c.2356G>T
|
XP_011529431.1:p.Ala786Ser
|
|
XM_011531130.1:c.2356G>T
|
XP_011529432.1:p.Ala786Ser
|
|
XM_011531131.1:c.2155G>T
|
XP_011529433.1:p.Ala719Ser
|
|
NM_001110556.2:c.2356G>T
MANE Select
|
NP_001104026.1:p.Ala786Ser
|
|
NM_001456.4:c.2356G>T
|
NP_001447.2:p.Ala786Ser
|
|