|
ENST00000645603.2:c.1272G>T
(THPO)
|
ENSP00000494281.2:p.Leu424=
|
|
|
ENST00000647395.1:c.852G>T
(THPO)
MANE Select
|
ENSP00000494504.1:p.Leu284=
|
|
|
ENST00000649095.1:c.1272G>T
(THPO)
|
ENSP00000497904.1:p.Leu424=
|
|
|
ENST00000650229.1:c.835G>T
(THPO)
|
ENSP00000497233.1:p.Ala279Ser
|
|
|
ENST00000204615.11:c.852G>T
(THPO)
|
ENSP00000204615.7:p.Leu284=
|
|
|
ENST00000421442.2:c.736G>T
(THPO)
|
ENSP00000411704.2:p.Ala246Ser
|
|
|
ENST00000444495.1:c.2106+228016C>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+228016C>A
|
|
|
ENST00000445696.6:c.840G>T
(THPO)
|
ENSP00000410763.2:p.Leu280=
|
|
|
NM_000460.3:c.852G>T
(THPO)
|
NP_000451.1:p.Leu284=
|
|
|
NM_001177597.2:c.840G>T
(THPO)
|
NP_001171068.1:p.Leu280=
|
|
|
NM_001177598.2:c.835G>T
(THPO)
|
NP_001171069.1:p.Ala279Ser
|
|
|
NM_001289997.1:c.736G>T
(THPO)
|
NP_001276926.1:p.Ala246Ser
|
|
|
NM_001289998.1:c.852G>T
(THPO)
|
NP_001276927.1:p.Leu284=
|
|
|
NM_001290003.1:c.1272G>T
(THPO)
|
NP_001276932.1:p.Leu424=
|
|
|
NM_001290022.1:c.840G>T
(THPO)
|
NP_001276951.1:p.Leu280=
|
|
|
NM_001290026.1:c.835G>T
(THPO)
|
NP_001276955.1:p.Ala279Ser
|
|
|
NM_001290027.1:c.736G>T
(THPO)
|
NP_001276956.1:p.Ala246Ser
|
|
|
NM_001290028.1:c.852G>T
(THPO)
|
NP_001276957.1:p.Leu284=
|
|
|
XM_011513113.1:c.1144G>T
(THPO)
|
XP_011511415.1:p.Ala382Ser
|
|
|
NM_000460.4:c.852G>T
(THPO)
MANE Select
|
NP_000451.1:p.Leu284=
|
|
|
XM_017007107.1:c.1144G>T
(THPO)
|
XP_016862596.1:p.Ala382Ser
|
|
