ENST00000561514.3:c.3411A>T
|
ENSP00000460666.3:p.Gly1137=
|
|
ENST00000565038.2:c.*890A>T
|
ENSP00000459882.2:n.*890A>T
|
|
ENST00000566069.6:c.*40A>T
|
ENSP00000459237.2:n.*40A>T
|
|
ENST00000697377.2:c.3249A>T
|
ENSP00000513286.2:p.Gly1083=
|
|
ENST00000697379.2:c.3411A>T
|
ENSP00000513287.2:p.Gly1137=
|
|
ENST00000561514.2:c.2520A>T
|
ENSP00000460666.2:p.Gly840=
|
|
ENST00000697374.1:c.2520A>T
|
ENSP00000513284.1:p.Gly840=
|
|
ENST00000697375.1:n.4752A>T
|
|
|
ENST00000697376.1:c.*40A>T
|
ENSP00000513285.1:n.*40A>T
|
|
ENST00000697377.1:c.2358A>T
|
ENSP00000513286.1:p.Gly786=
|
|
ENST00000697378.1:n.3925A>T
|
|
|
ENST00000697379.1:c.2520A>T
|
ENSP00000513287.1:p.Gly840=
|
|
ENST00000697380.1:n.2609A>T
|
|
|
ENST00000697381.1:n.2100A>T
|
|
|
ENST00000697382.1:c.*182A>T
|
ENSP00000513288.1:n.*182A>T
|
|
ENST00000697383.1:c.939A>T
|
ENSP00000513289.1:p.Gly313=
|
|
ENST00000261584.9:c.3405A>T
MANE Select
|
ENSP00000261584.4:p.Gly1135=
|
|
ENST00000261584.8:c.3405A>T
|
ENSP00000261584.4:p.Gly1135=
|
|
ENST00000566069.5:c.171A>T
|
|
|
ENST00000568219.5:c.2520A>T
|
ENSP00000454703.2:p.Gly840=
|
|
NM_024675.3:c.3405A>T , LRG_308t1:c.3405A>T
|
NP_078951.2:p.Gly1135=
|
|
XM_011545946.1:c.3411A>T
|
XP_011544248.1:p.Gly1137=
|
|
XM_011545947.1:c.*40A>T
|
XP_011544249.1:n.*40A>T
|
|
XM_011545948.1:c.2520A>T
|
XP_011544250.1:p.Gly840=
|
|
XR_950851.1:n.4113A>T
|
|
|
XM_011545946.2:c.3411A>T
|
XP_011544248.1:p.Gly1137=
|
|
XM_011545947.2:c.*40A>T
|
XP_011544249.1:n.*40A>T
|
|
XM_011545948.2:c.2520A>T
|
XP_011544250.1:p.Gly840=
|
|
XM_017023671.1:c.3174A>T
|
XP_016879160.1:p.Gly1058=
|
|
XM_017023672.2:c.3168A>T
|
XP_016879161.1:p.Gly1056=
|
|
XM_017023673.2:c.*40A>T
|
XP_016879162.1:n.*40A>T
|
|
NM_024675.4:c.3405A>T
MANE Select
|
NP_078951.2:p.Gly1135=
|
|