ENST00000319332.10:c.567G>A
MANE Select
|
ENSP00000316881.5:p.Glu189=
|
|
ENST00000319332.9:c.567G>A
|
ENSP00000316881.5:p.Glu189=
|
|
ENST00000426003.1:c.24G>A
|
ENSP00000394326.1:p.Glu8=
|
|
ENST00000427335.6:c.24G>A
|
ENSP00000408947.2:p.Glu8=
|
|
ENST00000444866.5:c.24G>A
|
ENSP00000391374.1:p.Glu8=
|
|
NM_001134418.1:c.24G>A
|
NP_001127890.1:p.Glu8=
|
|
NM_018192.3:c.567G>A
|
NP_060662.2:p.Glu189=
|
|
XM_011512955.1:c.24G>A
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XP_011511257.1:p.Glu8=
|
|
NM_018192.4:c.567G>A
MANE Select
|
NP_060662.2:p.Glu189=
|
|
NM_001134418.2:c.24G>A
|
NP_001127890.1:p.Glu8=
|
|