ENST00000478003.2:n.2289G>C
|
|
|
ENST00000682103.1:c.2G>C
|
|
|
ENST00000682276.1:n.1906G>C
|
|
|
ENST00000682892.1:c.2008G>C
|
ENSP00000507214.1:p.Glu670Gln
|
|
ENST00000682952.1:n.2100G>C
|
|
|
ENST00000684455.1:c.1674G>C
|
|
|
ENST00000684642.1:c.1858G>C
|
ENSP00000507355.1:p.Glu620Gln
|
|
ENST00000684740.1:n.2639G>C
|
|
|
ENST00000303236.9:c.2461G>C
MANE Select
|
ENSP00000307235.3:p.Glu821Gln
|
|
ENST00000652099.1:c.2655G>C
|
|
|
ENST00000652736.1:n.2337G>C
|
|
|
ENST00000303236.7:c.2461G>C
|
ENSP00000307235.3:p.Glu821Gln
|
|
ENST00000415570.1:c.2098G>C
|
ENSP00000412076.1:p.Glu700Gln
|
|
ENST00000419748.5:c.2008G>C
|
ENSP00000408325.1:p.Glu670Gln
|
|
ENST00000470706.1:n.104G>C
|
|
|
NM_001313915.1:c.2008G>C
|
NP_001300844.1:p.Glu670Gln
|
|
NM_004836.5:c.2461G>C
|
NP_004827.4:p.Glu821Gln
|
|
NM_004836.6:c.2461G>C
|
NP_004827.4:p.Glu821Gln
|
|
NR_110236.1:n.1159C>G
|
|
|
XM_005264649.3:c.1777G>C
|
XP_005264706.1:p.Glu593Gln
|
|
XM_017005376.2:c.1777G>C
|
XP_016860865.1:p.Glu593Gln
|
|
NM_004836.7:c.2461G>C
MANE Select
|
NP_004827.4:p.Glu821Gln
|
|
NM_001313915.2:c.2008G>C
|
NP_001300844.1:p.Glu670Gln
|
|