ENST00000298229.7:c.1098G>T
MANE Select
|
ENSP00000298229.2:p.Gln366His
|
|
ENST00000298229.6:c.1098G>T
|
ENSP00000298229.2:p.Gln366His
|
|
ENST00000538751.5:c.372G>T
|
ENSP00000444619.1:p.Gln124His
|
|
ENST00000540329.5:c.282G>T
|
ENSP00000440018.1:p.Gln94His
|
|
ENST00000541756.5:c.900G>T
|
ENSP00000446360.2:p.Gln300His
|
|
NM_001567.3:c.1098G>T
|
NP_001558.3:p.Gln366His
|
|
XM_005273978.3:c.1164G>T
|
XP_005274035.1:p.Gln388His
|
|
XM_005273979.3:c.1164G>T
|
XP_005274036.1:p.Gln388His
|
|
XM_011544999.1:c.1098G>T
|
XP_011543301.1:p.Gln366His
|
|
XM_011545000.1:c.1164G>T
|
XP_011543302.1:p.Gln388His
|
|
XM_005273979.4:c.1164G>T
|
XP_005274036.1:p.Gln388His
|
|
XM_011544999.2:c.1098G>T
|
XP_011543301.1:p.Gln366His
|
|
XM_024448501.1:c.1164G>T
|
XP_024304269.1:p.Gln388His
|
|
XM_024448502.1:c.1164G>T
|
XP_024304270.1:p.Gln388His
|
|
XM_024448503.1:c.1134G>T
|
XP_024304271.1:p.Gln378His
|
|
XM_024448504.1:c.1098G>T
|
XP_024304272.1:p.Gln366His
|
|
XM_024448505.1:c.1164G>T
|
XP_024304273.1:p.Gln388His
|
|
NM_001567.4:c.1098G>T
MANE Select
|
NP_001558.3:p.Gln366His
|
|