ENST00000350026.11:c.2846A>C
|
ENSP00000055163.8:p.Asn949Thr
|
|
ENST00000414678.8:c.2756A>C
|
ENSP00000412835.3:p.Asn919Thr
|
|
ENST00000637015.2:c.2846A>C
|
ENSP00000489729.2:p.Asn949Thr
|
|
ENST00000319584.11:c.860A>C
|
ENSP00000313006.7:p.Asn287Thr
|
|
ENST00000346085.10:c.2885A>C
|
ENSP00000344546.5:p.Asn962Thr
|
|
ENST00000350026.10:c.2597A>C
|
ENSP00000055163.7:p.Asn866Thr
|
|
ENST00000414678.7:c.1004A>C
|
ENSP00000412835.2:p.Asn335Thr
|
|
ENST00000452544.2:n.747A>C
|
|
|
ENST00000635849.1:c.167A>C
|
ENSP00000490948.1:p.Asn56Thr
|
|
ENST00000636930.2:c.2846A>C
MANE Select
|
ENSP00000490491.2:p.Asn949Thr
|
|
ENST00000637015.1:c.85A>C
|
|
|
ENST00000637810.1:c.347A>C
|
ENSP00000489636.1:p.Asn116Thr
|
|
ENST00000637904.1:c.347A>C
|
ENSP00000490550.1:p.Asn116Thr
|
|
ENST00000647938.1:c.2636A>C
|
ENSP00000498155.1:p.Asn879Thr
|
|
ENST00000674190.1:n.1595A>C
|
|
|
ENST00000319584.10:c.863A>C
|
ENSP00000313006.6:p.Asn288Thr
|
|
ENST00000346085.9:c.2636A>C
|
ENSP00000344546.4:p.Asn879Thr
|
|
ENST00000350026.9:c.2597A>C
|
ENSP00000055163.7:p.Asn866Thr
|
|
ENST00000414678.6:c.1004A>C
|
ENSP00000412835.2:p.Asn335Thr
|
|
ENST00000452544.1:n.693A>C
|
|
|
NM_017519.2:c.2597A>C
|
NP_059989.2:p.Asn866Thr
|
|
NM_020732.3:c.2636A>C
|
NP_065783.3:p.Asn879Thr
|
|
XM_005267069.3:c.2597A>C
|
XP_005267126.2:p.Asn866Thr
|
|
XM_011535984.1:c.1547A>C
|
XP_011534286.1:p.Asn516Thr
|
|
XM_011535985.1:c.1367A>C
|
XP_011534287.1:p.Asn456Thr
|
|
XM_011535986.1:c.1127A>C
|
XP_011534288.1:p.Asn376Thr
|
|
XM_011535987.1:c.746A>C
|
XP_011534289.1:p.Asn249Thr
|
|
XM_011535988.1:c.-20+15501A>C
|
XP_011534290.1:n.-20+15501A>C
|
|
NM_001346813.1:c.2597A>C
|
NP_001333742.1:p.Asn866Thr
|
|
NM_001363725.1:c.347A>C
|
NP_001350654.1:p.Asn116Thr
|
|
XM_011535984.2:c.2678A>C
|
XP_011534286.2:p.Asn893Thr
|
|
XM_011535988.3:c.-20+15501A>C
|
XP_011534290.1:n.-20+15501A>C
|
|
XM_017011103.2:c.2678A>C
|
XP_016866592.1:p.Asn893Thr
|
|
XM_017011104.1:c.2678A>C
|
XP_016866593.1:p.Asn893Thr
|
|
XM_017011105.2:c.2678A>C
|
XP_016866594.1:p.Asn893Thr
|
|
XM_017011106.2:c.2678A>C
|
XP_016866595.1:p.Asn893Thr
|
|
XM_017011107.2:c.2498A>C
|
XP_016866596.1:p.Asn833Thr
|
|
XR_002956289.1:n.2761A>C
|
|
|
NM_001363725.2:c.347A>C
|
NP_001350654.1:p.Asn116Thr
|
|
NM_001371656.1:c.2885A>C
|
NP_001358585.1:p.Asn962Thr
|
|
NM_001374820.1:c.2885A>C
|
NP_001361749.1:p.Asn962Thr
|
|
NM_001374828.1:c.2846A>C
MANE Select
|
NP_001361757.1:p.Asn949Thr
|
|
NM_017519.3:c.2846A>C
|
NP_059989.3:p.Asn949Thr
|
|