ENST00000698260.1:c.8912G>A
MANE Select
|
ENSP00000513632.1:p.Arg2971Gln
|
|
ENST00000685858.1:c.9092G>A
|
ENSP00000508756.1:p.Arg3031Gln
|
|
ENST00000261383.3:c.9050G>A
|
ENSP00000261383.3:p.Arg3017Gln
|
|
NM_017539.2:c.9050G>A
|
NP_060009.1:p.Arg3017Gln
|
|
XM_006721062.1:c.8912G>A
|
XP_006721125.1:p.Arg2971Gln
|
|
XM_011545882.1:c.8933G>A
|
XP_011544184.1:p.Arg2978Gln
|
|
XM_011545883.1:c.8933G>A
|
XP_011544185.1:p.Arg2978Gln
|
|
XM_011545884.1:c.8690G>A
|
XP_011544186.1:p.Arg2897Gln
|
|
XM_011545885.1:c.8933G>A
|
XP_011544187.1:p.Arg2978Gln
|
|
XM_011545886.1:c.7922G>A
|
XP_011544188.1:p.Arg2641Gln
|
|
XM_011545887.1:c.7130G>A
|
XP_011544189.1:p.Arg2377Gln
|
|
XM_011545888.1:c.6335G>A
|
XP_011544190.1:p.Arg2112Gln
|
|
XM_011545889.1:c.6335G>A
|
XP_011544191.1:p.Arg2112Gln
|
|
NM_001347886.1:c.8912G>A
|
NP_001334815.1:p.Arg2971Gln
|
|
XM_011545882.2:c.8933G>A
|
XP_011544184.1:p.Arg2978Gln
|
|
XM_011545885.3:c.8933G>A
|
XP_011544187.1:p.Arg2978Gln
|
|
XM_011545886.2:c.7922G>A
|
XP_011544188.1:p.Arg2641Gln
|
|
XM_011545888.2:c.6335G>A
|
XP_011544190.1:p.Arg2112Gln
|
|
XM_011545889.2:c.6335G>A
|
XP_011544191.1:p.Arg2112Gln
|
|
XM_017023426.1:c.8798G>A
|
XP_016878915.1:p.Arg2933Gln
|
|
XM_017023427.1:c.8690G>A
|
XP_016878916.1:p.Arg2897Gln
|
|
XM_017023428.1:c.8354G>A
|
XP_016878917.1:p.Arg2785Gln
|
|
XM_017023430.1:c.2987G>A
|
XP_016878919.1:p.Arg996Gln
|
|
XM_017023432.1:c.9092G>A
|
XP_016878921.1:p.Arg3031Gln
|
|
NM_001347886.2:c.8912G>A
MANE Select
|
NP_001334815.1:p.Arg2971Gln
|
|