ENST00000348974.5:c.1954G>T
|
ENSP00000330021.7:p.Asp652Tyr
|
|
ENST00000394236.9:c.1954G>T
MANE Select
|
ENSP00000377783.3:p.Asp652Tyr
|
|
ENST00000407433.6:c.1909G>T
|
ENSP00000385794.2:p.Asp637Tyr
|
|
ENST00000647936.1:c.*57G>T
|
ENSP00000496822.1:n.*57G>T
|
|
ENST00000648381.1:n.2122G>T
|
|
|
ENST00000648853.1:c.1912G>T
|
ENSP00000497262.1:p.Asp638Tyr
|
|
ENST00000650591.1:c.2050G>T
|
ENSP00000497376.1:p.Asp684Tyr
|
|
ENST00000394236.7:c.1954G>T
|
ENSP00000377783.3:p.Asp652Tyr
|
|
ENST00000407433.5:c.1561G>T
|
ENSP00000385794.1:p.Asp521Tyr
|
|
NM_000313.3:c.1954G>T , LRG_572t1:c.1954G>T
|
NP_000304.2:p.Asp652Tyr
|
|
NM_001314077.1:c.2050G>T , LRG_572t2:c.2050G>T
|
NP_001301006.1:p.Asp684Tyr
|
|
NM_000313.4:c.1954G>T
MANE Select
|
NP_000304.2:p.Asp652Tyr
|
|
NM_001314077.2:c.2050G>T
|
NP_001301006.1:p.Asp684Tyr
|
|