ENST00000342992.11:c.98618T>C
(TTN)
|
ENSP00000343764.6:p.Val32873Ala
|
|
ENST00000342175.11:c.79703T>C
(TTN)
|
ENSP00000340554.6:p.Val26568Ala
|
|
ENST00000359218.10:c.79502T>C
(TTN)
|
ENSP00000352154.5:p.Val26501Ala
|
|
ENST00000342175.10:c.79703T>C
(TTN)
|
ENSP00000340554.6:p.Val26568Ala
|
|
ENST00000342992.10:c.98618T>C
(TTN)
|
ENSP00000343764.6:p.Val32873Ala
|
|
ENST00000359218.9:c.79502T>C
(TTN)
|
ENSP00000352154.5:p.Val26501Ala
|
|
ENST00000460472.6:c.79127T>C
(TTN)
|
ENSP00000434586.1:p.Val26376Ala
|
|
ENST00000589042.5:c.106322T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val35441Ala
|
|
ENST00000591111.5:c.101399T>C
(TTN)
|
ENSP00000465570.1:p.Val33800Ala
|
|
ENST00000615779.4:c.101399T>C
(TTN)
|
ENSP00000483597.1:p.Val33800Ala
|
|
NM_001256850.1:c.101399T>C
(TTN)
|
NP_001243779.1:p.Val33800Ala
|
|
NM_001267550.2:c.106322T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val35441Ala
|
|
NM_003319.4:c.79127T>C
(TTN)
|
NP_003310.4:p.Val26376Ala
|
|
NM_133378.4:c.98618T>C
(TTN)
|
NP_596869.4:p.Val32873Ala
|
|
NM_133432.3:c.79502T>C
(TTN)
|
NP_597676.3:p.Val26501Ala
|
|
NM_133437.4:c.79703T>C
(TTN)
|
NP_597681.4:p.Val26568Ala
|
|
NR_038271.1:n.446+6657A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5439A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105419T>C
(TTN)
|
XP_011510031.1:p.Val35140Ala
|
|
XM_011511730.1:c.79313T>C
(TTN)
|
XP_011510032.1:p.Val26438Ala
|
|
XM_011511731.1:c.79172T>C
(TTN)
|
XP_011510033.1:p.Val26391Ala
|
|
XM_017004819.1:c.105215T>C
(TTN)
|
XP_016860308.1:p.Val35072Ala
|
|
XM_017004820.1:c.100613T>C
(TTN)
|
XP_016860309.1:p.Val33538Ala
|
|
XM_017004821.1:c.100610T>C
(TTN)
|
XP_016860310.1:p.Val33537Ala
|
|
XM_017004822.1:c.97652T>C
(TTN)
|
XP_016860311.1:p.Val32551Ala
|
|
XM_017004823.1:c.79268T>C
(TTN)
|
XP_016860312.1:p.Val26423Ala
|
|
XM_024453094.1:c.100763T>C
(TTN)
|
XP_024308862.1:p.Val33588Ala
|
|
XM_024453095.1:c.100760T>C
(TTN)
|
XP_024308863.1:p.Val33587Ala
|
|
XM_024453096.1:c.100193T>C
(TTN)
|
XP_024308864.1:p.Val33398Ala
|
|
XM_024453097.1:c.97535T>C
(TTN)
|
XP_024308865.1:p.Val32512Ala
|
|
XM_024453098.1:c.97454T>C
(TTN)
|
XP_024308866.1:p.Val32485Ala
|
|
XM_024453099.1:c.79217T>C
(TTN)
|
XP_024308867.1:p.Val26406Ala
|
|
XM_024453100.1:c.69071T>C
(TTN)
|
XP_024308868.1:p.Val23024Ala
|
|