ENST00000342992.11:c.96900C>A
(TTN)
|
ENSP00000343764.6:p.Tyr32300Ter
|
|
ENST00000342175.11:c.77985C>A
(TTN)
|
ENSP00000340554.6:p.Tyr25995Ter
|
|
ENST00000359218.10:c.77784C>A
(TTN)
|
ENSP00000352154.5:p.Tyr25928Ter
|
|
ENST00000342175.10:c.77985C>A
(TTN)
|
ENSP00000340554.6:p.Tyr25995Ter
|
|
ENST00000342992.10:c.96900C>A
(TTN)
|
ENSP00000343764.6:p.Tyr32300Ter
|
|
ENST00000359218.9:c.77784C>A
(TTN)
|
ENSP00000352154.5:p.Tyr25928Ter
|
|
ENST00000460472.6:c.77409C>A
(TTN)
|
ENSP00000434586.1:p.Tyr25803Ter
|
|
ENST00000589042.5:c.104604C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr34868Ter
|
|
ENST00000591111.5:c.99681C>A
(TTN)
|
ENSP00000465570.1:p.Tyr33227Ter
|
|
ENST00000615779.4:c.99681C>A
(TTN)
|
ENSP00000483597.1:p.Tyr33227Ter
|
|
NM_001256850.1:c.99681C>A
(TTN)
|
NP_001243779.1:p.Tyr33227Ter
|
|
NM_001267550.2:c.104604C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr34868Ter
|
|
NM_003319.4:c.77409C>A
(TTN)
|
NP_003310.4:p.Tyr25803Ter
|
|
NM_133378.4:c.96900C>A
(TTN)
|
NP_596869.4:p.Tyr32300Ter
|
|
NM_133432.3:c.77784C>A
(TTN)
|
NP_597676.3:p.Tyr25928Ter
|
|
NM_133437.4:c.77985C>A
(TTN)
|
NP_597681.4:p.Tyr25995Ter
|
|
NR_038271.1:n.446+8375G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3721G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103701C>A
(TTN)
|
XP_011510031.1:p.Tyr34567Ter
|
|
XM_011511730.1:c.77595C>A
(TTN)
|
XP_011510032.1:p.Tyr25865Ter
|
|
XM_011511731.1:c.77454C>A
(TTN)
|
XP_011510033.1:p.Tyr25818Ter
|
|
XM_017004819.1:c.103497C>A
(TTN)
|
XP_016860308.1:p.Tyr34499Ter
|
|
XM_017004820.1:c.98895C>A
(TTN)
|
XP_016860309.1:p.Tyr32965Ter
|
|
XM_017004821.1:c.98892C>A
(TTN)
|
XP_016860310.1:p.Tyr32964Ter
|
|
XM_017004822.1:c.95934C>A
(TTN)
|
XP_016860311.1:p.Tyr31978Ter
|
|
XM_017004823.1:c.77550C>A
(TTN)
|
XP_016860312.1:p.Tyr25850Ter
|
|
XM_024453094.1:c.99045C>A
(TTN)
|
XP_024308862.1:p.Tyr33015Ter
|
|
XM_024453095.1:c.99042C>A
(TTN)
|
XP_024308863.1:p.Tyr33014Ter
|
|
XM_024453096.1:c.98475C>A
(TTN)
|
XP_024308864.1:p.Tyr32825Ter
|
|
XM_024453097.1:c.95817C>A
(TTN)
|
XP_024308865.1:p.Tyr31939Ter
|
|
XM_024453098.1:c.95736C>A
(TTN)
|
XP_024308866.1:p.Tyr31912Ter
|
|
XM_024453099.1:c.77499C>A
(TTN)
|
XP_024308867.1:p.Tyr25833Ter
|
|
XM_024453100.1:c.67353C>A
(TTN)
|
XP_024308868.1:p.Tyr22451Ter
|
|