ENST00000391944.8:c.1935G>C
|
ENSP00000375808.4:p.Gln645His
|
|
ENST00000682414.1:c.1935G>C
|
ENSP00000507019.1:p.Gln645His
|
|
ENST00000682508.1:n.1964G>C
|
|
|
ENST00000684218.1:c.*1193G>C
|
ENSP00000507804.1:n.*1193G>C
|
|
ENST00000684264.1:n.1491G>C
|
|
|
ENST00000684407.1:c.1812G>C
|
ENSP00000507775.1:p.Gln604His
|
|
ENST00000684458.1:c.*421G>C
|
ENSP00000508260.1:n.*421G>C
|
|
ENST00000684468.1:n.1647G>C
|
|
|
ENST00000391945.10:c.1935G>C
MANE Select
|
ENSP00000375809.4:p.Gln645His
|
|
ENST00000646507.1:n.2032G>C
|
|
|
ENST00000391941.6:c.1863G>C
|
ENSP00000375805.2:p.Gln621His
|
|
ENST00000391942.6:n.1106G>C
|
|
|
ENST00000391944.7:c.1701G>C
|
ENSP00000375808.3:p.Gln567His
|
|
ENST00000391945.8:c.1935G>C
|
ENSP00000375809.3:p.Gln645His
|
|
ENST00000588652.5:n.2023G>C
|
|
|
NM_000400.3:c.1935G>C , LRG_461t1:c.1935G>C
|
NP_000391.1:p.Gln645His
|
|
XM_011526611.1:c.1857G>C
|
XP_011524913.1:p.Gln619His
|
|
XM_011526611.2:c.1857G>C
|
XP_011524913.1:p.Gln619His
|
|
XM_017026467.1:c.1812G>C
|
XP_016881956.1:p.Gln604His
|
|
XR_001753633.2:n.1982G>C
|
|
|
XR_001753634.2:n.1918G>C
|
|
|
NM_000400.4:c.1935G>C
MANE Select
|
NP_000391.1:p.Gln645His
|
|