ENST00000247933.9:c.1683A>C
|
ENSP00000247933.4:p.Gln561His
|
|
ENST00000514224.2:c.1683A>C
MANE Select
|
ENSP00000425081.2:p.Gln561His
|
|
ENST00000652070.1:n.1739A>C
|
|
|
ENST00000247933.8:c.1683A>C
|
ENSP00000247933.4:p.Gln561His
|
|
ENST00000514224.1:c.1287A>C
|
ENSP00000425081.1:p.Gln429His
|
|
ENST00000514417.1:n.75A>C
|
|
|
ENST00000514698.5:n.1790A>C
|
|
|
NM_000203.4:c.1683A>C
|
NP_000194.2:p.Gln561His
|
|
NR_110313.1:n.1771A>C
|
|
|
XM_006713882.2:c.1287A>C
|
XP_006713945.1:p.Gln429His
|
|
XM_011513459.1:c.1749A>C
|
XP_011511761.1:p.Gln583His
|
|
XM_011513460.1:c.1542A>C
|
XP_011511762.1:p.Gln514His
|
|
XM_011513461.1:c.1476A>C
|
XP_011511763.1:p.Gln492His
|
|
XM_011513462.1:c.1395A>C
|
XP_011511764.1:p.Gln465His
|
|
XM_011513463.1:c.1395A>C
|
XP_011511765.1:p.Gln465His
|
|
XR_924947.1:n.1939A>C
|
|
|
NM_000203.5:c.1683A>C
MANE Select
|
NP_000194.2:p.Gln561His
|
|
NM_001363576.1:c.1287A>C
|
NP_001350505.1:p.Gln429His
|
|
XM_011513461.2:c.1476A>C
|
XP_011511763.1:p.Gln492His
|
|
XM_017008163.1:c.723A>C
|
XP_016863652.1:p.Gln241His
|
|