ENST00000313468.10:c.429T>C
MANE Select
|
ENSP00000315774.5:p.Tyr143=
|
|
ENST00000313468.9:c.429T>C
|
ENSP00000315774.5:p.Tyr143=
|
|
ENST00000524810.5:c.361T>C
|
|
|
ENST00000525419.5:c.375T>C
|
ENSP00000433521.1:p.Tyr125=
|
|
ENST00000526339.5:c.429T>C
|
ENSP00000436287.1:p.Tyr143=
|
|
ENST00000526446.5:c.*484T>C
|
ENSP00000433645.1:n.*484T>C
|
|
ENST00000528492.1:c.-10T>C
|
ENSP00000432848.1:n.-10T>C
|
|
ENST00000531282.1:n.281T>C
|
|
|
NM_002496.3:c.429T>C
|
NP_002487.1:p.Tyr143=
|
|
XM_005274013.1:c.429T>C
|
XP_005274070.1:p.Tyr143=
|
|
XM_005274014.1:c.429T>C
|
XP_005274071.1:p.Tyr143=
|
|
XM_005274015.1:c.309T>C
|
XP_005274072.1:p.Tyr103=
|
|
XM_011545053.1:c.429T>C
|
XP_011543355.1:p.Tyr143=
|
|
NM_002496.4:c.429T>C
MANE Select
|
NP_002487.1:p.Tyr143=
|
|