ENST00000247933.9:c.1210G>A
|
ENSP00000247933.4:p.Glu404Lys
|
|
ENST00000514224.2:c.1210G>A
MANE Select
|
ENSP00000425081.2:p.Glu404Lys
|
|
ENST00000652070.1:n.1266G>A
|
|
|
ENST00000247933.8:c.1210G>A
|
ENSP00000247933.4:p.Glu404Lys
|
|
ENST00000502829.1:n.12G>A
|
|
|
ENST00000514224.1:c.814G>A
|
ENSP00000425081.1:p.Glu272Lys
|
|
ENST00000514698.5:n.1317G>A
|
|
|
NM_000203.4:c.1210G>A
|
NP_000194.2:p.Glu404Lys
|
|
NR_110313.1:n.1298G>A
|
|
|
XM_006713882.2:c.814G>A
|
XP_006713945.1:p.Glu272Lys
|
|
XM_011513459.1:c.1276G>A
|
XP_011511761.1:p.Glu426Lys
|
|
XM_011513460.1:c.1069G>A
|
XP_011511762.1:p.Glu357Lys
|
|
XM_011513461.1:c.1003G>A
|
XP_011511763.1:p.Glu335Lys
|
|
XM_011513462.1:c.922G>A
|
XP_011511764.1:p.Glu308Lys
|
|
XM_011513463.1:c.922G>A
|
XP_011511765.1:p.Glu308Lys
|
|
XR_924947.1:n.1279G>A
|
|
|
NM_000203.5:c.1210G>A
MANE Select
|
NP_000194.2:p.Glu404Lys
|
|
NM_001363576.1:c.814G>A
|
NP_001350505.1:p.Glu272Lys
|
|
XM_011513461.2:c.1003G>A
|
XP_011511763.1:p.Glu335Lys
|
|
XM_017008163.1:c.250G>A
|
XP_016863652.1:p.Glu84Lys
|
|