ENST00000642948.1:c.1695A>C
MANE Select
|
ENSP00000496347.1:p.Glu565Asp
|
|
ENST00000335730.6:n.1008A>C
|
|
|
ENST00000441551.6:c.1695A>C
|
ENSP00000387621.2:p.Glu565Asp
|
|
ENST00000536736.5:c.1695A>C
|
ENSP00000444586.1:p.Glu565Asp
|
|
NM_144612.6:c.1695A>C
|
NP_653213.6:p.Glu565Asp
|
|
XM_011525803.1:c.1695A>C
|
XP_011524105.1:p.Glu565Asp
|
|
XM_011525804.1:c.-30-1877A>C
|
XP_011524106.1:n.-30-1877A>C
|
|
XM_011525804.2:c.-30-1877A>C
|
XP_011524106.1:n.-30-1877A>C
|
|
XM_017025548.1:c.1695A>C
|
XP_016881037.1:p.Glu565Asp
|
|
XM_024451084.1:c.177A>C
|
XP_024306852.1:p.Glu59Asp
|
|
NM_001384474.1:c.1695A>C
MANE Select
|
NP_001371403.1:p.Glu565Asp
|
|
NM_144612.7:c.1695A>C
|
NP_653213.6:p.Glu565Asp
|
|