ENST00000645603.2:c.1212C>A
(THPO)
|
ENSP00000494281.2:p.Pro404=
|
|
ENST00000647395.1:c.792C>A
(THPO)
MANE Select
|
ENSP00000494504.1:p.Pro264=
|
|
ENST00000649095.1:c.1212C>A
(THPO)
|
ENSP00000497904.1:p.Pro404=
|
|
ENST00000650229.1:c.775C>A
(THPO)
|
ENSP00000497233.1:p.Leu259Ile
|
|
ENST00000204615.11:c.792C>A
(THPO)
|
ENSP00000204615.7:p.Pro264=
|
|
ENST00000421442.2:c.676C>A
(THPO)
|
ENSP00000411704.2:p.Leu226Ile
|
|
ENST00000444495.1:c.2106+228076G>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+228076G>T
|
|
ENST00000445696.6:c.780C>A
(THPO)
|
ENSP00000410763.2:p.Pro260=
|
|
NM_000460.3:c.792C>A
(THPO)
|
NP_000451.1:p.Pro264=
|
|
NM_001177597.2:c.780C>A
(THPO)
|
NP_001171068.1:p.Pro260=
|
|
NM_001177598.2:c.775C>A
(THPO)
|
NP_001171069.1:p.Leu259Ile
|
|
NM_001289997.1:c.676C>A
(THPO)
|
NP_001276926.1:p.Leu226Ile
|
|
NM_001289998.1:c.792C>A
(THPO)
|
NP_001276927.1:p.Pro264=
|
|
NM_001290003.1:c.1212C>A
(THPO)
|
NP_001276932.1:p.Pro404=
|
|
NM_001290022.1:c.780C>A
(THPO)
|
NP_001276951.1:p.Pro260=
|
|
NM_001290026.1:c.775C>A
(THPO)
|
NP_001276955.1:p.Leu259Ile
|
|
NM_001290027.1:c.676C>A
(THPO)
|
NP_001276956.1:p.Leu226Ile
|
|
NM_001290028.1:c.792C>A
(THPO)
|
NP_001276957.1:p.Pro264=
|
|
XM_011513113.1:c.1084C>A
(THPO)
|
XP_011511415.1:p.Leu362Ile
|
|
NM_000460.4:c.792C>A
(THPO)
MANE Select
|
NP_000451.1:p.Pro264=
|
|
XM_017007107.1:c.1084C>A
(THPO)
|
XP_016862596.1:p.Leu362Ile
|
|