ENST00000478003.2:n.2297A>G
|
|
|
ENST00000682103.1:c.10A>G
|
|
|
ENST00000682276.1:n.1914A>G
|
|
|
ENST00000682892.1:c.2016A>G
|
ENSP00000507214.1:p.Lys672=
|
|
ENST00000682952.1:n.2108A>G
|
|
|
ENST00000684455.1:c.1682A>G
|
|
|
ENST00000684642.1:c.1866A>G
|
ENSP00000507355.1:p.Lys622=
|
|
ENST00000684740.1:n.2647A>G
|
|
|
ENST00000303236.9:c.2469A>G
MANE Select
|
ENSP00000307235.3:p.Lys823=
|
|
ENST00000652099.1:c.2663A>G
|
|
|
ENST00000652736.1:n.2345A>G
|
|
|
ENST00000303236.7:c.2469A>G
|
ENSP00000307235.3:p.Lys823=
|
|
ENST00000415570.1:c.2106A>G
|
ENSP00000412076.1:p.Lys702=
|
|
ENST00000419748.5:c.2016A>G
|
ENSP00000408325.1:p.Lys672=
|
|
ENST00000470706.1:n.112A>G
|
|
|
NM_001313915.1:c.2016A>G
|
NP_001300844.1:p.Lys672=
|
|
NM_004836.5:c.2469A>G
|
NP_004827.4:p.Lys823=
|
|
NM_004836.6:c.2469A>G
|
NP_004827.4:p.Lys823=
|
|
NR_110236.1:n.1151T>C
|
|
|
XM_005264649.3:c.1785A>G
|
XP_005264706.1:p.Lys595=
|
|
XM_017005376.2:c.1785A>G
|
XP_016860865.1:p.Lys595=
|
|
NM_004836.7:c.2469A>G
MANE Select
|
NP_004827.4:p.Lys823=
|
|
NM_001313915.2:c.2016A>G
|
NP_001300844.1:p.Lys672=
|
|