ENST00000697291.1:c.*64A>C
|
ENSP00000513228.1:n.*64A>C
|
|
ENST00000648433.1:c.467A>C
|
ENSP00000496816.1:p.Glu156Ala
|
|
ENST00000649554.1:n.77A>C
|
|
|
ENST00000649979.2:c.467A>C
MANE Select
|
ENSP00000497271.1:p.Glu156Ala
|
|
ENST00000679938.1:c.302A>C
|
ENSP00000505518.1:p.Glu101Ala
|
|
ENST00000263642.2:c.467A>C
|
ENSP00000263642.2:p.Glu156Ala
|
|
ENST00000421365.2:c.467A>C
|
ENSP00000408450.2:p.Glu156Ala
|
|
NM_022168.3:c.467A>C
|
NP_071451.2:p.Glu156Ala
|
|
XM_011511629.1:c.467A>C
|
XP_011509931.1:p.Glu156Ala
|
|
NM_022168.4:c.467A>C
MANE Select
|
NP_071451.2:p.Glu156Ala
|
|