|
ENST00000682275.1:c.2221G>C
|
ENSP00000507852.1:p.Asp741His
|
|
|
ENST00000683395.1:c.2162G>C
|
|
|
|
ENST00000684087.1:c.2185G>C
|
ENSP00000506978.1:p.Asp729His
|
|
|
ENST00000506362.2:c.1936G>C
|
ENSP00000424103.2:p.Asp646His
|
|
|
ENST00000673642.1:c.1844G>C
|
ENSP00000501242.1:n.1844G>C
|
|
|
ENST00000673991.1:c.2221G>C
|
ENSP00000501033.1:p.Asp741His
|
|
|
ENST00000226760.5:c.2185G>C
MANE Select
|
ENSP00000226760.1:p.Asp729His
|
|
|
ENST00000503569.5:c.2185G>C
|
ENSP00000423337.1:p.Asp729His
|
|
|
ENST00000507765.1:n.2370G>C
|
|
|
|
NM_001145853.1:c.2185G>C
|
NP_001139325.1:p.Asp729His
|
|
|
NM_006005.3:c.2185G>C
MANE Select
|
NP_005996.2:p.Asp729His
|
|
|
XM_017008586.1:c.2194G>C
|
XP_016864075.1:p.Asp732His
|
|
