|
ENST00000561514.3:c.1478C>T
|
ENSP00000460666.3:p.Ala493Val
|
|
|
ENST00000565038.2:c.211+2776C>T
|
ENSP00000459882.2:n.211+2776C>T
|
|
|
ENST00000566069.6:c.1472C>T
|
ENSP00000459237.2:p.Ala491Val
|
|
|
ENST00000697377.2:c.1478C>T
|
ENSP00000513286.2:p.Ala493Val
|
|
|
ENST00000697379.2:c.1478C>T
|
ENSP00000513287.2:p.Ala493Val
|
|
|
ENST00000561514.2:c.587C>T
|
ENSP00000460666.2:p.Ala196Val
|
|
|
ENST00000697374.1:c.587C>T
|
ENSP00000513284.1:p.Ala196Val
|
|
|
ENST00000697375.1:n.2819C>T
|
|
|
|
ENST00000697376.1:c.587C>T
|
ENSP00000513285.1:p.Ala196Val
|
|
|
ENST00000697377.1:c.587C>T
|
ENSP00000513286.1:p.Ala196Val
|
|
|
ENST00000697378.1:n.1992C>T
|
|
|
|
ENST00000697379.1:c.587C>T
|
ENSP00000513287.1:p.Ala196Val
|
|
|
ENST00000697382.1:c.587C>T
|
ENSP00000513288.1:p.Ala196Val
|
|
|
ENST00000697383.1:c.49-5799C>T
|
ENSP00000513289.1:n.49-5799C>T
|
|
|
ENST00000697384.1:n.1626C>T
|
|
|
|
ENST00000261584.9:c.1472C>T
MANE Select
|
ENSP00000261584.4:p.Ala491Val
|
|
|
ENST00000261584.8:c.1472C>T
|
ENSP00000261584.4:p.Ala491Val
|
|
|
ENST00000565038.1:c.86+2776C>T
|
|
|
|
ENST00000568219.5:c.587C>T
|
ENSP00000454703.2:p.Ala196Val
|
|
|
NM_024675.3:c.1472C>T , LRG_308t1:c.1472C>T
|
NP_078951.2:p.Ala491Val
|
|
|
XM_011545946.1:c.1478C>T
|
XP_011544248.1:p.Ala493Val
|
|
|
XM_011545947.1:c.1478C>T
|
XP_011544249.1:p.Ala493Val
|
|
|
XM_011545948.1:c.587C>T
|
XP_011544250.1:p.Ala196Val
|
|
|
XR_950851.1:n.2268C>T
|
|
|
|
XM_011545946.2:c.1478C>T
|
XP_011544248.1:p.Ala493Val
|
|
|
XM_011545947.2:c.1478C>T
|
XP_011544249.1:p.Ala493Val
|
|
|
XM_011545948.2:c.587C>T
|
XP_011544250.1:p.Ala196Val
|
|
|
XM_017023671.1:c.1478C>T
|
XP_016879160.1:p.Ala493Val
|
|
|
XM_017023672.2:c.1472C>T
|
XP_016879161.1:p.Ala491Val
|
|
|
XM_017023673.2:c.1472C>T
|
XP_016879162.1:p.Ala491Val
|
|
|
NM_024675.4:c.1472C>T
MANE Select
|
NP_078951.2:p.Ala491Val
|
|
