|
ENST00000359206.8:c.3753G>C
|
ENSP00000352135.3:p.Lys1251Asn
|
|
|
ENST00000649586.2:c.3753G>C
MANE Select
|
ENSP00000496956.2:p.Lys1251Asn
|
|
|
ENST00000265723.8:c.3774G>C
|
ENSP00000265723.4:p.Lys1258Asn
|
|
|
ENST00000358400.7:c.3612G>C
|
ENSP00000351172.3:p.Lys1204Asn
|
|
|
ENST00000359206.7:c.3753G>C
|
ENSP00000352135.3:p.Lys1251Asn
|
|
|
ENST00000440025.1:c.187G>C
|
|
|
|
ENST00000453593.5:c.3612G>C
|
ENSP00000392983.1:p.Lys1204Asn
|
|
|
ENST00000467983.1:n.365G>C
|
|
|
|
NM_000443.3:c.3753G>C
|
NP_000434.1:p.Lys1251Asn
|
|
|
NM_018849.2:c.3774G>C
|
NP_061337.1:p.Lys1258Asn
|
|
|
NM_018850.2:c.3612G>C
|
NP_061338.1:p.Lys1204Asn
|
|
|
XM_011516308.1:c.3774G>C
|
XP_011514610.1:p.Lys1258Asn
|
|
|
XM_011516309.1:c.3753G>C
|
XP_011514611.1:p.Lys1251Asn
|
|
|
XM_011516310.1:c.3669G>C
|
XP_011514612.1:p.Lys1223Asn
|
|
|
XM_011516311.1:c.3645G>C
|
XP_011514613.1:p.Lys1215Asn
|
|
|
XM_011516312.1:c.3633G>C
|
XP_011514614.1:p.Lys1211Asn
|
|
|
XM_011516313.1:c.3612G>C
|
XP_011514615.1:p.Lys1204Asn
|
|
|
XM_011516314.1:c.3795G>C
|
XP_011514616.1:p.Lys1265Asn
|
|
|
XM_011516315.1:c.3114G>C
|
XP_011514617.1:p.Lys1038Asn
|
|
|
XM_011516308.3:c.4044G>C
|
XP_011514610.3:p.Lys1348Asn
|
|
|
XM_011516309.3:c.4023G>C
|
XP_011514611.3:p.Lys1341Asn
|
|
|
XM_011516310.3:c.3939G>C
|
XP_011514612.3:p.Lys1313Asn
|
|
|
XM_011516311.3:c.3915G>C
|
XP_011514613.3:p.Lys1305Asn
|
|
|
XM_011516312.3:c.3903G>C
|
XP_011514614.3:p.Lys1301Asn
|
|
|
XM_011516313.3:c.3882G>C
|
XP_011514615.2:p.Lys1294Asn
|
|
|
XM_011516315.3:c.3114G>C
|
XP_011514617.2:p.Lys1038Asn
|
|
|
XM_017012323.2:c.3774G>C
|
XP_016867812.1:p.Lys1258Asn
|
|
|
XR_001744809.2:n.4282G>C
|
|
|
|
NM_000443.4:c.3753G>C
MANE Select
|
NP_000434.1:p.Lys1251Asn
|
|
|
NM_018849.3:c.3774G>C
|
NP_061337.1:p.Lys1258Asn
|
|
|
NM_018850.3:c.3612G>C
|
NP_061338.1:p.Lys1204Asn
|
|
