ENST00000342992.11:c.100234G>C
(TTN)
|
ENSP00000343764.6:p.Asp33412His
|
|
ENST00000342175.11:c.81319G>C
(TTN)
|
ENSP00000340554.6:p.Asp27107His
|
|
ENST00000359218.10:c.81118G>C
(TTN)
|
ENSP00000352154.5:p.Asp27040His
|
|
ENST00000342175.10:c.81319G>C
(TTN)
|
ENSP00000340554.6:p.Asp27107His
|
|
ENST00000342992.10:c.100234G>C
(TTN)
|
ENSP00000343764.6:p.Asp33412His
|
|
ENST00000359218.9:c.81118G>C
(TTN)
|
ENSP00000352154.5:p.Asp27040His
|
|
ENST00000460472.6:c.80743G>C
(TTN)
|
ENSP00000434586.1:p.Asp26915His
|
|
ENST00000589042.5:c.107938G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35980His
|
|
ENST00000591111.5:c.103015G>C
(TTN)
|
ENSP00000465570.1:p.Asp34339His
|
|
ENST00000615779.4:c.103015G>C
(TTN)
|
ENSP00000483597.1:p.Asp34339His
|
|
NM_001256850.1:c.103015G>C
(TTN)
|
NP_001243779.1:p.Asp34339His
|
|
NM_001267550.2:c.107938G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35980His
|
|
NM_003319.4:c.80743G>C
(TTN)
|
NP_003310.4:p.Asp26915His
|
|
NM_133378.4:c.100234G>C
(TTN)
|
NP_596869.4:p.Asp33412His
|
|
NM_133432.3:c.81118G>C
(TTN)
|
NP_597676.3:p.Asp27040His
|
|
NM_133437.4:c.81319G>C
(TTN)
|
NP_597681.4:p.Asp27107His
|
|
NR_038271.1:n.446+3414C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3414C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.107035G>C
(TTN)
|
XP_011510031.1:p.Asp35679His
|
|
XM_011511730.1:c.80929G>C
(TTN)
|
XP_011510032.1:p.Asp26977His
|
|
XM_011511731.1:c.80788G>C
(TTN)
|
XP_011510033.1:p.Asp26930His
|
|
XM_017004819.1:c.106831G>C
(TTN)
|
XP_016860308.1:p.Asp35611His
|
|
XM_017004820.1:c.102229G>C
(TTN)
|
XP_016860309.1:p.Asp34077His
|
|
XM_017004821.1:c.102226G>C
(TTN)
|
XP_016860310.1:p.Asp34076His
|
|
XM_017004822.1:c.99268G>C
(TTN)
|
XP_016860311.1:p.Asp33090His
|
|
XM_017004823.1:c.80884G>C
(TTN)
|
XP_016860312.1:p.Asp26962His
|
|
XM_024453094.1:c.102379G>C
(TTN)
|
XP_024308862.1:p.Asp34127His
|
|
XM_024453095.1:c.102376G>C
(TTN)
|
XP_024308863.1:p.Asp34126His
|
|
XM_024453096.1:c.101809G>C
(TTN)
|
XP_024308864.1:p.Asp33937His
|
|
XM_024453097.1:c.99151G>C
(TTN)
|
XP_024308865.1:p.Asp33051His
|
|
XM_024453098.1:c.99070G>C
(TTN)
|
XP_024308866.1:p.Asp33024His
|
|
XM_024453099.1:c.80833G>C
(TTN)
|
XP_024308867.1:p.Asp26945His
|
|
XM_024453100.1:c.70687G>C
(TTN)
|
XP_024308868.1:p.Asp23563His
|
|