ENST00000478003.2:n.2272A>C
|
|
|
ENST00000682276.1:n.1889A>C
|
|
|
ENST00000682892.1:c.1991A>C
|
ENSP00000507214.1:p.Asn664Thr
|
|
ENST00000682952.1:n.2083A>C
|
|
|
ENST00000684455.1:c.1657A>C
|
|
|
ENST00000684642.1:c.1841A>C
|
ENSP00000507355.1:p.Asn614Thr
|
|
ENST00000684740.1:n.2622A>C
|
|
|
ENST00000303236.9:c.2444A>C
MANE Select
|
ENSP00000307235.3:p.Asn815Thr
|
|
ENST00000652099.1:c.2638A>C
|
|
|
ENST00000652736.1:n.2320A>C
|
|
|
ENST00000303236.7:c.2444A>C
|
ENSP00000307235.3:p.Asn815Thr
|
|
ENST00000415570.1:c.2081A>C
|
ENSP00000412076.1:p.Asn694Thr
|
|
ENST00000419748.5:c.1991A>C
|
ENSP00000408325.1:p.Asn664Thr
|
|
ENST00000470706.1:n.87A>C
|
|
|
NM_001313915.1:c.1991A>C
|
NP_001300844.1:p.Asn664Thr
|
|
NM_004836.5:c.2444A>C
|
NP_004827.4:p.Asn815Thr
|
|
NM_004836.6:c.2444A>C
|
NP_004827.4:p.Asn815Thr
|
|
NR_110236.1:n.1176T>G
|
|
|
XM_005264649.3:c.1760A>C
|
XP_005264706.1:p.Asn587Thr
|
|
XM_017005376.2:c.1760A>C
|
XP_016860865.1:p.Asn587Thr
|
|
NM_004836.7:c.2444A>C
MANE Select
|
NP_004827.4:p.Asn815Thr
|
|
NM_001313915.2:c.1991A>C
|
NP_001300844.1:p.Asn664Thr
|
|