ENST00000527168.6:n.633A>C
|
|
|
ENST00000529110.2:c.618A>C
|
ENSP00000435349.2:p.Pro206=
|
|
ENST00000529957.6:n.592A>C
|
|
|
ENST00000683366.1:c.*266A>C
|
ENSP00000507283.1:n.*266A>C
|
|
ENST00000683887.1:c.582A>C
|
ENSP00000506886.1:p.Pro194=
|
|
ENST00000684100.1:n.528A>C
|
|
|
ENST00000684126.1:n.592A>C
|
|
|
ENST00000684688.1:n.1159A>C
|
|
|
ENST00000204679.9:c.534A>C
MANE Select
|
ENSP00000204679.4:p.Pro178=
|
|
ENST00000204679.8:c.534A>C
|
ENSP00000204679.4:p.Pro178=
|
|
ENST00000527076.1:n.1681A>C
|
|
|
ENST00000527168.5:n.701A>C
|
|
|
ENST00000529957.5:n.633A>C
|
|
|
NM_032520.4:c.534A>C
|
NP_115909.1:p.Pro178=
|
|
XM_017023782.1:c.582A>C
|
XP_016879271.1:p.Pro194=
|
|
XM_017023783.1:c.174A>C
|
XP_016879272.1:p.Pro58=
|
|
NM_032520.5:c.534A>C
MANE Select
|
NP_115909.1:p.Pro178=
|
|