ENST00000247933.9:c.1275C>A
|
ENSP00000247933.4:p.His425Gln
|
|
ENST00000514224.2:c.1275C>A
MANE Select
|
ENSP00000425081.2:p.His425Gln
|
|
ENST00000652070.1:n.1331C>A
|
|
|
ENST00000247933.8:c.1275C>A
|
ENSP00000247933.4:p.His425Gln
|
|
ENST00000502829.1:n.77C>A
|
|
|
ENST00000514224.1:c.879C>A
|
ENSP00000425081.1:p.His293Gln
|
|
ENST00000514698.5:n.1382C>A
|
|
|
NM_000203.4:c.1275C>A
|
NP_000194.2:p.His425Gln
|
|
NR_110313.1:n.1363C>A
|
|
|
XM_006713882.2:c.879C>A
|
XP_006713945.1:p.His293Gln
|
|
XM_011513459.1:c.1341C>A
|
XP_011511761.1:p.His447Gln
|
|
XM_011513460.1:c.1134C>A
|
XP_011511762.1:p.His378Gln
|
|
XM_011513461.1:c.1068C>A
|
XP_011511763.1:p.His356Gln
|
|
XM_011513462.1:c.987C>A
|
XP_011511764.1:p.His329Gln
|
|
XM_011513463.1:c.987C>A
|
XP_011511765.1:p.His329Gln
|
|
XR_924947.1:n.1344C>A
|
|
|
NM_000203.5:c.1275C>A
MANE Select
|
NP_000194.2:p.His425Gln
|
|
NM_001363576.1:c.879C>A
|
NP_001350505.1:p.His293Gln
|
|
XM_011513461.2:c.1068C>A
|
XP_011511763.1:p.His356Gln
|
|
XM_017008163.1:c.315C>A
|
XP_016863652.1:p.His105Gln
|
|