ENST00000236671.7:c.590G>C
MANE Select
|
ENSP00000236671.2:p.Gly197Ala
|
|
ENST00000367196.4:c.485G>C
|
ENSP00000356164.4:p.Gly162Ala
|
|
ENST00000427721.3:c.15G>C
|
|
|
ENST00000429746.2:c.485G>C
|
ENSP00000402586.2:p.Gly162Ala
|
|
ENST00000433655.6:c.590G>C
|
ENSP00000404902.1:p.Gly197Ala
|
|
ENST00000438213.6:c.590G>C
|
ENSP00000415036.2:p.Gly197Ala
|
|
ENST00000636397.1:c.590G>C
|
ENSP00000489910.1:p.Gly197Ala
|
|
ENST00000636571.1:c.569G>C
|
ENSP00000490770.1:p.Gly190Ala
|
|
ENST00000636615.1:c.590G>C
|
ENSP00000490014.1:p.Gly197Ala
|
|
ENST00000636843.1:c.584G>C
|
ENSP00000490897.1:p.Gly195Ala
|
|
ENST00000637158.1:n.188G>C
|
|
|
ENST00000637381.2:n.3018G>C
|
|
|
ENST00000637387.1:c.590G>C
|
ENSP00000490598.1:p.Gly197Ala
|
|
ENST00000637815.2:c.590G>C
|
ENSP00000490344.1:p.Gly197Ala
|
|
ENST00000637915.1:c.590G>C
|
ENSP00000490471.1:p.Gly197Ala
|
|
ENST00000677300.1:n.985G>C
|
|
|
ENST00000678991.1:c.*451G>C
|
ENSP00000503019.1:n.*451G>C
|
|
ENST00000236671.6:c.590G>C
|
ENSP00000236671.2:p.Gly197Ala
|
|
ENST00000367196.3:c.485G>C
|
ENSP00000356164.3:p.Gly162Ala
|
|
ENST00000427721.2:c.-11G>C
|
ENSP00000415840.2:n.-11G>C
|
|
ENST00000433655.5:c.590G>C
|
ENSP00000404902.1:p.Gly197Ala
|
|
ENST00000438213.5:c.545G>C
|
ENSP00000415036.1:p.Gly182Ala
|
|
NM_001909.4:c.590G>C
|
NP_001900.1:p.Gly197Ala
|
|
NM_001909.5:c.590G>C
MANE Select
|
NP_001900.1:p.Gly197Ala
|
|