ENST00000636937.2:c.1762G>C
|
ENSP00000516154.1:p.Gly588Arg
|
|
ENST00000268124.11:c.1762G>C
MANE Select
|
ENSP00000268124.5:p.Gly588Arg
|
|
ENST00000530292.3:c.1363G>C
|
ENSP00000432885.2:p.Gly455Arg
|
|
ENST00000635986.2:c.1762G>C
|
ENSP00000490653.2:p.Gly588Arg
|
|
ENST00000636774.1:c.*329G>C
|
ENSP00000489799.1:n.*329G>C
|
|
ENST00000637238.1:c.499G>C
|
ENSP00000490756.1:p.Gly167Arg
|
|
ENST00000637264.1:c.834G>C
|
|
|
ENST00000666746.1:c.1339G>C
|
|
|
ENST00000670281.1:c.82G>C
|
ENSP00000499709.1:p.Gly28Arg
|
|
ENST00000672071.1:n.1960G>C
|
|
|
ENST00000672923.2:n.1865G>C
|
|
|
ENST00000268124.9:c.1762G>C
|
ENSP00000268124.5:p.Gly588Arg
|
|
ENST00000442287.6:c.1762G>C
|
ENSP00000399851.2:p.Gly588Arg
|
|
ENST00000526314.2:c.144G>C
|
|
|
ENST00000631044.2:c.*1145G>C
|
ENSP00000486730.1:n.*1145G>C
|
|
NM_001126131.1:c.1762G>C
|
NP_001119603.1:p.Gly588Arg
|
|
NM_002693.2:c.1762G>C
|
NP_002684.1:p.Gly588Arg
|
|
NM_001126131.2:c.1762G>C
|
NP_001119603.1:p.Gly588Arg
|
|
NM_002693.3:c.1762G>C
MANE Select
|
NP_002684.1:p.Gly588Arg
|
|