ENST00000703118.1:c.*2902T>C
|
ENSP00000515181.1:n.*2902T>C
|
|
ENST00000703131.1:n.3445T>C
|
|
|
ENST00000703139.1:c.2315T>C
|
|
|
ENST00000703140.1:c.7314T>C
|
ENSP00000515197.1:p.Thr2438=
|
|
ENST00000703141.1:c.*3044T>C
|
ENSP00000515198.1:n.*3044T>C
|
|
ENST00000703142.1:c.*4357T>C
|
ENSP00000515199.1:n.*4357T>C
|
|
ENST00000361445.9:c.7527T>C
MANE Select
|
ENSP00000354558.4:p.Thr2509=
|
|
ENST00000361445.8:c.7527T>C
|
ENSP00000354558.4:p.Thr2509=
|
|
ENST00000376838.5:c.2142T>C
|
ENSP00000366034.1:p.Thr714=
|
|
ENST00000473471.5:n.539T>C
|
|
|
ENST00000490931.1:n.810T>C
|
|
|
NM_004958.3:c.7527T>C , LRG_734t1:c.7527T>C
|
NP_004949.1:p.Thr2509=
|
|
XM_005263438.1:c.7527T>C
|
XP_005263495.1:p.Thr2509=
|
|
XM_005263438.2:c.7527T>C
|
XP_005263495.1:p.Thr2509=
|
|
XM_017000900.1:c.6846T>C
|
XP_016856389.1:p.Thr2282=
|
|
XM_017000901.1:c.6279T>C
|
XP_016856390.1:p.Thr2093=
|
|
XM_024446187.1:c.7527T>C
|
XP_024301955.1:p.Thr2509=
|
|
XR_001737087.1:n.7565T>C
|
|
|
NM_004958.4:c.7527T>C
MANE Select
|
NP_004949.1:p.Thr2509=
|
|
NM_001386500.1:c.7527T>C
|
NP_001373429.1:p.Thr2509=
|
|
NM_001386501.1:c.6279T>C
|
NP_001373430.1:p.Thr2093=
|
|