ENST00000527168.6:n.419T>G
|
|
|
ENST00000529110.2:c.404T>G
|
ENSP00000435349.2:p.Ile135Ser
|
|
ENST00000529957.6:n.378T>G
|
|
|
ENST00000683366.1:c.*52T>G
|
ENSP00000507283.1:n.*52T>G
|
|
ENST00000683887.1:c.368T>G
|
ENSP00000506886.1:p.Ile123Ser
|
|
ENST00000684100.1:n.314T>G
|
|
|
ENST00000684126.1:n.378T>G
|
|
|
ENST00000684688.1:n.945T>G
|
|
|
ENST00000204679.9:c.320T>G
MANE Select
|
ENSP00000204679.4:p.Ile107Ser
|
|
ENST00000204679.8:c.320T>G
|
ENSP00000204679.4:p.Ile107Ser
|
|
ENST00000526820.5:c.*222T>G
|
ENSP00000434413.1:n.*222T>G
|
|
ENST00000527076.1:n.1336T>G
|
|
|
ENST00000527168.5:n.356T>G
|
|
|
ENST00000529110.1:c.387T>G
|
|
|
ENST00000529957.5:n.419T>G
|
|
|
NM_032520.4:c.320T>G
|
NP_115909.1:p.Ile107Ser
|
|
XM_017023782.1:c.368T>G
|
XP_016879271.1:p.Ile123Ser
|
|
XM_017023783.1:c.-41T>G
|
XP_016879272.1:n.-41T>G
|
|
NM_032520.5:c.320T>G
MANE Select
|
NP_115909.1:p.Ile107Ser
|
|