ENST00000247933.9:c.987T>A
|
ENSP00000247933.4:p.His329Gln
|
|
ENST00000514224.2:c.987T>A
MANE Select
|
ENSP00000425081.2:p.His329Gln
|
|
ENST00000652070.1:n.1043T>A
|
|
|
ENST00000247933.8:c.987T>A
|
ENSP00000247933.4:p.His329Gln
|
|
ENST00000514224.1:c.591T>A
|
ENSP00000425081.1:p.His197Gln
|
|
ENST00000514698.5:n.1094T>A
|
|
|
NM_000203.4:c.987T>A
|
NP_000194.2:p.His329Gln
|
|
NR_110313.1:n.1075T>A
|
|
|
XM_006713882.2:c.591T>A
|
XP_006713945.1:p.His197Gln
|
|
XM_011513459.1:c.1053T>A
|
XP_011511761.1:p.His351Gln
|
|
XM_011513460.1:c.846T>A
|
XP_011511762.1:p.His282Gln
|
|
XM_011513461.1:c.780T>A
|
XP_011511763.1:p.His260Gln
|
|
XM_011513462.1:c.699T>A
|
XP_011511764.1:p.His233Gln
|
|
XM_011513463.1:c.699T>A
|
XP_011511765.1:p.His233Gln
|
|
XR_924947.1:n.1056T>A
|
|
|
NM_000203.5:c.987T>A
MANE Select
|
NP_000194.2:p.His329Gln
|
|
NM_001363576.1:c.591T>A
|
NP_001350505.1:p.His197Gln
|
|
XM_011513461.2:c.780T>A
|
XP_011511763.1:p.His260Gln
|
|
XM_017008163.1:c.27T>A
|
XP_016863652.1:p.His9Gln
|
|