ENST00000247933.9:c.1279C>A
|
ENSP00000247933.4:p.Pro427Thr
|
|
ENST00000514224.2:c.1279C>A
MANE Select
|
ENSP00000425081.2:p.Pro427Thr
|
|
ENST00000652070.1:n.1335C>A
|
|
|
ENST00000247933.8:c.1279C>A
|
ENSP00000247933.4:p.Pro427Thr
|
|
ENST00000502829.1:n.81C>A
|
|
|
ENST00000514224.1:c.883C>A
|
ENSP00000425081.1:p.Pro295Thr
|
|
ENST00000514698.5:n.1386C>A
|
|
|
NM_000203.4:c.1279C>A
|
NP_000194.2:p.Pro427Thr
|
|
NR_110313.1:n.1367C>A
|
|
|
XM_006713882.2:c.883C>A
|
XP_006713945.1:p.Pro295Thr
|
|
XM_011513459.1:c.1345C>A
|
XP_011511761.1:p.Pro449Thr
|
|
XM_011513460.1:c.1138C>A
|
XP_011511762.1:p.Pro380Thr
|
|
XM_011513461.1:c.1072C>A
|
XP_011511763.1:p.Pro358Thr
|
|
XM_011513462.1:c.991C>A
|
XP_011511764.1:p.Pro331Thr
|
|
XM_011513463.1:c.991C>A
|
XP_011511765.1:p.Pro331Thr
|
|
XR_924947.1:n.1348C>A
|
|
|
NM_000203.5:c.1279C>A
MANE Select
|
NP_000194.2:p.Pro427Thr
|
|
NM_001363576.1:c.883C>A
|
NP_001350505.1:p.Pro295Thr
|
|
XM_011513461.2:c.1072C>A
|
XP_011511763.1:p.Pro358Thr
|
|
XM_017008163.1:c.319C>A
|
XP_016863652.1:p.Pro107Thr
|
|