ENST00000636937.2:c.1736G>C
|
ENSP00000516154.1:p.Arg579Pro
|
|
ENST00000268124.11:c.1736G>C
MANE Select
|
ENSP00000268124.5:p.Arg579Pro
|
|
ENST00000530292.3:c.1337G>C
|
ENSP00000432885.2:p.Arg446Pro
|
|
ENST00000635986.2:c.1736G>C
|
ENSP00000490653.2:p.Arg579Pro
|
|
ENST00000636774.1:c.*303G>C
|
ENSP00000489799.1:n.*303G>C
|
|
ENST00000637238.1:c.473G>C
|
ENSP00000490756.1:p.Arg158Pro
|
|
ENST00000637264.1:c.808G>C
|
|
|
ENST00000666746.1:c.1313G>C
|
|
|
ENST00000670281.1:c.56G>C
|
ENSP00000499709.1:p.Arg19Pro
|
|
ENST00000672071.1:n.1934G>C
|
|
|
ENST00000672923.2:n.1839G>C
|
|
|
ENST00000268124.9:c.1736G>C
|
ENSP00000268124.5:p.Arg579Pro
|
|
ENST00000442287.6:c.1736G>C
|
ENSP00000399851.2:p.Arg579Pro
|
|
ENST00000526314.2:c.118G>C
|
|
|
ENST00000631044.2:c.*1119G>C
|
ENSP00000486730.1:n.*1119G>C
|
|
NM_001126131.1:c.1736G>C
|
NP_001119603.1:p.Arg579Pro
|
|
NM_002693.2:c.1736G>C
|
NP_002684.1:p.Arg579Pro
|
|
NM_001126131.2:c.1736G>C
|
NP_001119603.1:p.Arg579Pro
|
|
NM_002693.3:c.1736G>C
MANE Select
|
NP_002684.1:p.Arg579Pro
|
|