ENST00000247933.9:c.572T>C
|
ENSP00000247933.4:p.Val191Ala
|
|
ENST00000514224.2:c.572T>C
MANE Select
|
ENSP00000425081.2:p.Val191Ala
|
|
ENST00000652070.1:n.628T>C
|
|
|
ENST00000247933.8:c.572T>C
|
ENSP00000247933.4:p.Val191Ala
|
|
ENST00000502910.5:c.431T>C
|
ENSP00000422952.1:p.Val144Ala
|
|
ENST00000504568.5:c.532T>C
|
|
|
ENST00000509948.5:c.365T>C
|
ENSP00000424227.1:p.Val122Ala
|
|
ENST00000514192.5:c.389T>C
|
ENSP00000423685.1:p.Val130Ala
|
|
ENST00000514224.1:c.176T>C
|
ENSP00000425081.1:p.Val59Ala
|
|
ENST00000514698.5:n.472T>C
|
|
|
NM_000203.4:c.572T>C
|
NP_000194.2:p.Val191Ala
|
|
NR_110313.1:n.660T>C
|
|
|
XM_006713882.2:c.176T>C
|
XP_006713945.1:p.Val59Ala
|
|
XM_011513459.1:c.431T>C
|
XP_011511761.1:p.Val144Ala
|
|
XM_011513460.1:c.431T>C
|
XP_011511762.1:p.Val144Ala
|
|
XM_011513461.1:c.365T>C
|
XP_011511763.1:p.Val122Ala
|
|
XM_011513462.1:c.284T>C
|
XP_011511764.1:p.Val95Ala
|
|
XM_011513463.1:c.284T>C
|
XP_011511765.1:p.Val95Ala
|
|
XR_924947.1:n.641T>C
|
|
|
NM_000203.5:c.572T>C
MANE Select
|
NP_000194.2:p.Val191Ala
|
|
NM_001363576.1:c.176T>C
|
NP_001350505.1:p.Val59Ala
|
|
XM_011513461.2:c.365T>C
|
XP_011511763.1:p.Val122Ala
|
|
XM_017008163.1:c.-417T>C
|
XP_016863652.1:n.-417T>C
|
|