ENST00000342992.11:c.98625T>G
(TTN)
|
ENSP00000343764.6:p.Ala32875=
|
|
ENST00000342175.11:c.79710T>G
(TTN)
|
ENSP00000340554.6:p.Ala26570=
|
|
ENST00000359218.10:c.79509T>G
(TTN)
|
ENSP00000352154.5:p.Ala26503=
|
|
ENST00000342175.10:c.79710T>G
(TTN)
|
ENSP00000340554.6:p.Ala26570=
|
|
ENST00000342992.10:c.98625T>G
(TTN)
|
ENSP00000343764.6:p.Ala32875=
|
|
ENST00000359218.9:c.79509T>G
(TTN)
|
ENSP00000352154.5:p.Ala26503=
|
|
ENST00000460472.6:c.79134T>G
(TTN)
|
ENSP00000434586.1:p.Ala26378=
|
|
ENST00000589042.5:c.106329T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35443=
|
|
ENST00000591111.5:c.101406T>G
(TTN)
|
ENSP00000465570.1:p.Ala33802=
|
|
ENST00000615779.4:c.101406T>G
(TTN)
|
ENSP00000483597.1:p.Ala33802=
|
|
NM_001256850.1:c.101406T>G
(TTN)
|
NP_001243779.1:p.Ala33802=
|
|
NM_001267550.2:c.106329T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35443=
|
|
NM_003319.4:c.79134T>G
(TTN)
|
NP_003310.4:p.Ala26378=
|
|
NM_133378.4:c.98625T>G
(TTN)
|
NP_596869.4:p.Ala32875=
|
|
NM_133432.3:c.79509T>G
(TTN)
|
NP_597676.3:p.Ala26503=
|
|
NM_133437.4:c.79710T>G
(TTN)
|
NP_597681.4:p.Ala26570=
|
|
NR_038271.1:n.446+6650A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5446A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105426T>G
(TTN)
|
XP_011510031.1:p.Ala35142=
|
|
XM_011511730.1:c.79320T>G
(TTN)
|
XP_011510032.1:p.Ala26440=
|
|
XM_011511731.1:c.79179T>G
(TTN)
|
XP_011510033.1:p.Ala26393=
|
|
XM_017004819.1:c.105222T>G
(TTN)
|
XP_016860308.1:p.Ala35074=
|
|
XM_017004820.1:c.100620T>G
(TTN)
|
XP_016860309.1:p.Ala33540=
|
|
XM_017004821.1:c.100617T>G
(TTN)
|
XP_016860310.1:p.Ala33539=
|
|
XM_017004822.1:c.97659T>G
(TTN)
|
XP_016860311.1:p.Ala32553=
|
|
XM_017004823.1:c.79275T>G
(TTN)
|
XP_016860312.1:p.Ala26425=
|
|
XM_024453094.1:c.100770T>G
(TTN)
|
XP_024308862.1:p.Ala33590=
|
|
XM_024453095.1:c.100767T>G
(TTN)
|
XP_024308863.1:p.Ala33589=
|
|
XM_024453096.1:c.100200T>G
(TTN)
|
XP_024308864.1:p.Ala33400=
|
|
XM_024453097.1:c.97542T>G
(TTN)
|
XP_024308865.1:p.Ala32514=
|
|
XM_024453098.1:c.97461T>G
(TTN)
|
XP_024308866.1:p.Ala32487=
|
|
XM_024453099.1:c.79224T>G
(TTN)
|
XP_024308867.1:p.Ala26408=
|
|
XM_024453100.1:c.69078T>G
(TTN)
|
XP_024308868.1:p.Ala23026=
|
|