|
ENST00000561514.3:c.3304A=
|
ENSP00000460666.3:p.Thr1102=
|
|
|
ENST00000565038.2:c.*779A=
|
ENSP00000459882.2:n.*779A=
|
|
|
ENST00000566069.6:c.3202-4247A=
|
ENSP00000459237.2:n.3202-4247A=
|
|
|
ENST00000697377.2:c.3142A=
|
ENSP00000513286.2:p.Thr1048=
|
|
|
ENST00000697379.2:c.3304A=
|
ENSP00000513287.2:p.Thr1102=
|
|
|
ENST00000561514.2:c.2413A=
|
ENSP00000460666.2:p.Thr805=
|
|
|
ENST00000697374.1:c.2413A=
|
ENSP00000513284.1:p.Thr805=
|
|
|
ENST00000697375.1:n.4645A=
|
|
|
|
ENST00000697376.1:c.2317-4247A=
|
ENSP00000513285.1:n.2317-4247A=
|
|
|
ENST00000697377.1:c.2251A=
|
ENSP00000513286.1:p.Thr751=
|
|
|
ENST00000697378.1:n.3818A=
|
|
|
|
ENST00000697379.1:c.2413A=
|
ENSP00000513287.1:p.Thr805=
|
|
|
ENST00000697380.1:n.2502A=
|
|
|
|
ENST00000697381.1:n.1993A=
|
|
|
|
ENST00000697382.1:c.*75A=
|
ENSP00000513288.1:n.*75A=
|
|
|
ENST00000697383.1:c.832A=
|
ENSP00000513289.1:p.Thr278=
|
|
|
ENST00000261584.9:c.3298A=
MANE Select
|
ENSP00000261584.4:p.Thr1100=
|
|
|
ENST00000261584.8:c.3298A=
|
ENSP00000261584.4:p.Thr1100=
|
|
|
ENST00000566069.5:c.117-4247A=
|
|
|
|
ENST00000568219.5:c.2413A=
|
ENSP00000454703.2:p.Thr805=
|
|
|
NM_024675.3:c.3298A= , LRG_308t1:c.3298A=
|
NP_078951.2:p.Thr1100=
|
|
|
XM_011545946.1:c.3304A=
|
XP_011544248.1:p.Thr1102=
|
|
|
XM_011545947.1:c.3208-4247A=
|
XP_011544249.1:n.3208-4247A=
|
|
|
XM_011545948.1:c.2413A=
|
XP_011544250.1:p.Thr805=
|
|
|
XR_950851.1:n.4006A=
|
|
|
|
XM_011545946.2:c.3304A=
|
XP_011544248.1:p.Thr1102=
|
|
|
XM_011545947.2:c.3208-4247A=
|
XP_011544249.1:n.3208-4247A=
|
|
|
XM_011545948.2:c.2413A=
|
XP_011544250.1:p.Thr805=
|
|
|
XM_017023671.1:c.3120-4247A=
|
XP_016879160.1:n.3120-4247A=
|
|
|
XM_017023672.2:c.3114-4247A=
|
XP_016879161.1:n.3114-4247A=
|
|
|
XM_017023673.2:c.3202-4247A=
|
XP_016879162.1:n.3202-4247A=
|
|
|
NM_024675.4:c.3298A=
MANE Select
|
NP_078951.2:p.Thr1100=
|
|
