ENST00000526189.3:c.544G>T
|
ENSP00000488104.2:p.Ala182Ser
|
|
ENST00000533357.5:c.625G>T
MANE Select
|
ENSP00000432943.1:p.Ala209Ser
|
|
ENST00000672287.2:c.37G>T
|
ENSP00000499818.2:p.Ala13Ser
|
|
ENST00000672602.2:c.625G>T
|
ENSP00000500814.2:p.Ala209Ser
|
|
ENST00000674861.1:n.688G>T
|
|
|
ENST00000463290.5:c.625G>T
|
ENSP00000431538.1:p.Ala209Ser
|
|
ENST00000476410.1:n.85G>T
|
|
|
ENST00000488271.1:n.63G>T
|
|
|
ENST00000491222.5:c.37G>T
|
ENSP00000431441.1:p.Ala13Ser
|
|
ENST00000526189.2:c.288G>T
|
|
|
ENST00000533357.4:c.625G>T
|
ENSP00000432943.1:p.Ala209Ser
|
|
NM_000530.6:c.625G>T , LRG_256t1:c.625G>T
|
NP_000521.2:p.Ala209Ser
|
|
NM_000530.7:c.625G>T
|
NP_000521.2:p.Ala209Ser
|
|
NM_001315491.1:c.625G>T
|
NP_001302420.1:p.Ala209Ser
|
|
XM_017001321.2:c.655G>T
|
XP_016856810.1:p.Ala219Ser
|
|
NM_000530.8:c.625G>T
MANE Select
|
NP_000521.2:p.Ala209Ser
|
|
NM_001315491.2:c.625G>T
|
NP_001302420.1:p.Ala209Ser
|
|