ENST00000301071.12:c.384G>C
MANE Select
|
ENSP00000301071.7:p.Gln128His
|
|
ENST00000547939.6:c.279G>C
|
ENSP00000450268.2:p.Gln93His
|
|
ENST00000550767.6:c.279G>C
|
ENSP00000446637.1:p.Gln93His
|
|
ENST00000550811.2:n.1417G>C
|
|
|
ENST00000552924.2:c.279G>C
|
ENSP00000448725.2:p.Gln93His
|
|
ENST00000679733.1:c.407G>C
|
ENSP00000505459.1:p.Ser136Thr
|
|
ENST00000295766.9:c.384G>C
|
ENSP00000439020.2:p.Gln128His
|
|
ENST00000301071.11:c.384G>C
|
ENSP00000301071.7:p.Gln128His
|
|
ENST00000546918.1:c.536G>C
|
ENSP00000446613.1:p.Ser179Thr
|
|
ENST00000547939.5:c.279G>C
|
ENSP00000450268.1:p.Gln93His
|
|
ENST00000550767.5:c.279G>C
|
ENSP00000446637.1:p.Gln93His
|
|
ENST00000552924.1:c.279G>C
|
ENSP00000448725.1:p.Gln93His
|
|
NM_001270399.1:c.384G>C
|
NP_001257328.1:p.Gln128His
|
|
NM_001270400.1:c.279G>C
|
NP_001257329.1:p.Gln93His
|
|
NM_006009.3:c.384G>C
|
NP_006000.2:p.Gln128His
|
|
NM_006009.4:c.384G>C
MANE Select
|
NP_006000.2:p.Gln128His
|
|
NM_001270399.2:c.384G>C
|
NP_001257328.1:p.Gln128His
|
|
NM_001270400.2:c.279G>C
|
NP_001257329.1:p.Gln93His
|
|