ENST00000645603.2:c.1263A>C
(THPO)
|
ENSP00000494281.2:p.Thr421=
|
|
ENST00000647395.1:c.843A>C
(THPO)
MANE Select
|
ENSP00000494504.1:p.Thr281=
|
|
ENST00000649095.1:c.1263A>C
(THPO)
|
ENSP00000497904.1:p.Thr421=
|
|
ENST00000650229.1:c.826A>C
(THPO)
|
ENSP00000497233.1:p.Arg276=
|
|
ENST00000204615.11:c.843A>C
(THPO)
|
ENSP00000204615.7:p.Thr281=
|
|
ENST00000421442.2:c.727A>C
(THPO)
|
ENSP00000411704.2:p.Arg243=
|
|
ENST00000444495.1:c.2106+228025T>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+228025T>G
|
|
ENST00000445696.6:c.831A>C
(THPO)
|
ENSP00000410763.2:p.Thr277=
|
|
NM_000460.3:c.843A>C
(THPO)
|
NP_000451.1:p.Thr281=
|
|
NM_001177597.2:c.831A>C
(THPO)
|
NP_001171068.1:p.Thr277=
|
|
NM_001177598.2:c.826A>C
(THPO)
|
NP_001171069.1:p.Arg276=
|
|
NM_001289997.1:c.727A>C
(THPO)
|
NP_001276926.1:p.Arg243=
|
|
NM_001289998.1:c.843A>C
(THPO)
|
NP_001276927.1:p.Thr281=
|
|
NM_001290003.1:c.1263A>C
(THPO)
|
NP_001276932.1:p.Thr421=
|
|
NM_001290022.1:c.831A>C
(THPO)
|
NP_001276951.1:p.Thr277=
|
|
NM_001290026.1:c.826A>C
(THPO)
|
NP_001276955.1:p.Arg276=
|
|
NM_001290027.1:c.727A>C
(THPO)
|
NP_001276956.1:p.Arg243=
|
|
NM_001290028.1:c.843A>C
(THPO)
|
NP_001276957.1:p.Thr281=
|
|
XM_011513113.1:c.1135A>C
(THPO)
|
XP_011511415.1:p.Arg379=
|
|
NM_000460.4:c.843A>C
(THPO)
MANE Select
|
NP_000451.1:p.Thr281=
|
|
XM_017007107.1:c.1135A>C
(THPO)
|
XP_016862596.1:p.Arg379=
|
|