ENST00000527168.6:n.841G>T
|
|
|
ENST00000529110.2:c.826G>T
|
ENSP00000435349.2:p.Ala276Ser
|
|
ENST00000529957.6:n.800G>T
|
|
|
ENST00000683366.1:c.*474G>T
|
ENSP00000507283.1:n.*474G>T
|
|
ENST00000683887.1:c.790G>T
|
ENSP00000506886.1:p.Ala264Ser
|
|
ENST00000684100.1:n.736G>T
|
|
|
ENST00000684126.1:n.876G>T
|
|
|
ENST00000684688.1:n.1367G>T
|
|
|
ENST00000204679.9:c.742G>T
MANE Select
|
ENSP00000204679.4:p.Ala248Ser
|
|
ENST00000204679.8:c.742G>T
|
ENSP00000204679.4:p.Ala248Ser
|
|
ENST00000527076.1:n.1965G>T
|
|
|
ENST00000527168.5:n.909G>T
|
|
|
ENST00000529957.5:n.841G>T
|
|
|
NM_032520.4:c.742G>T
|
NP_115909.1:p.Ala248Ser
|
|
XM_017023782.1:c.790G>T
|
XP_016879271.1:p.Ala264Ser
|
|
XM_017023783.1:c.382G>T
|
XP_016879272.1:p.Ala128Ser
|
|
NM_032520.5:c.742G>T
MANE Select
|
NP_115909.1:p.Ala248Ser
|
|