ENST00000635540.2:c.*197G>A
|
ENSP00000489185.1:n.*197G>A
|
|
ENST00000399799.3:c.3562G>A
MANE Select
|
ENSP00000382697.1:p.Glu1188Lys
|
|
ENST00000399799.2:c.3562G>A
|
ENSP00000382697.1:p.Glu1188Lys
|
|
ENST00000584687.1:n.272G>A
|
|
|
ENST00000635540.1:c.*197G>A
|
ENSP00000489185.1:n.*197G>A
|
|
NM_005406.2:c.3562G>A
|
NP_005397.1:p.Glu1188Lys
|
|
XM_011526136.1:c.3640G>A
|
XP_011524438.1:p.Glu1214Lys
|
|
XM_011526137.1:c.2173G>A
|
XP_011524439.1:p.Glu725Lys
|
|
XM_011526137.3:c.2173G>A
|
XP_011524439.1:p.Glu725Lys
|
|
NM_005406.3:c.3562G>A
MANE Select
|
NP_005397.1:p.Glu1188Lys
|
|