ENST00000342992.11:c.98285G>C
(TTN)
|
ENSP00000343764.6:p.Gly32762Ala
|
|
ENST00000342175.11:c.79370G>C
(TTN)
|
ENSP00000340554.6:p.Gly26457Ala
|
|
ENST00000359218.10:c.79169G>C
(TTN)
|
ENSP00000352154.5:p.Gly26390Ala
|
|
ENST00000342175.10:c.79370G>C
(TTN)
|
ENSP00000340554.6:p.Gly26457Ala
|
|
ENST00000342992.10:c.98285G>C
(TTN)
|
ENSP00000343764.6:p.Gly32762Ala
|
|
ENST00000359218.9:c.79169G>C
(TTN)
|
ENSP00000352154.5:p.Gly26390Ala
|
|
ENST00000460472.6:c.78794G>C
(TTN)
|
ENSP00000434586.1:p.Gly26265Ala
|
|
ENST00000589042.5:c.105989G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35330Ala
|
|
ENST00000591111.5:c.101066G>C
(TTN)
|
ENSP00000465570.1:p.Gly33689Ala
|
|
ENST00000615779.4:c.101066G>C
(TTN)
|
ENSP00000483597.1:p.Gly33689Ala
|
|
NM_001256850.1:c.101066G>C
(TTN)
|
NP_001243779.1:p.Gly33689Ala
|
|
NM_001267550.2:c.105989G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35330Ala
|
|
NM_003319.4:c.78794G>C
(TTN)
|
NP_003310.4:p.Gly26265Ala
|
|
NM_133378.4:c.98285G>C
(TTN)
|
NP_596869.4:p.Gly32762Ala
|
|
NM_133432.3:c.79169G>C
(TTN)
|
NP_597676.3:p.Gly26390Ala
|
|
NM_133437.4:c.79370G>C
(TTN)
|
NP_597681.4:p.Gly26457Ala
|
|
NR_038271.1:n.446+6990C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5106C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105086G>C
(TTN)
|
XP_011510031.1:p.Gly35029Ala
|
|
XM_011511730.1:c.78980G>C
(TTN)
|
XP_011510032.1:p.Gly26327Ala
|
|
XM_011511731.1:c.78839G>C
(TTN)
|
XP_011510033.1:p.Gly26280Ala
|
|
XM_017004819.1:c.104882G>C
(TTN)
|
XP_016860308.1:p.Gly34961Ala
|
|
XM_017004820.1:c.100280G>C
(TTN)
|
XP_016860309.1:p.Gly33427Ala
|
|
XM_017004821.1:c.100277G>C
(TTN)
|
XP_016860310.1:p.Gly33426Ala
|
|
XM_017004822.1:c.97319G>C
(TTN)
|
XP_016860311.1:p.Gly32440Ala
|
|
XM_017004823.1:c.78935G>C
(TTN)
|
XP_016860312.1:p.Gly26312Ala
|
|
XM_024453094.1:c.100430G>C
(TTN)
|
XP_024308862.1:p.Gly33477Ala
|
|
XM_024453095.1:c.100427G>C
(TTN)
|
XP_024308863.1:p.Gly33476Ala
|
|
XM_024453096.1:c.99860G>C
(TTN)
|
XP_024308864.1:p.Gly33287Ala
|
|
XM_024453097.1:c.97202G>C
(TTN)
|
XP_024308865.1:p.Gly32401Ala
|
|
XM_024453098.1:c.97121G>C
(TTN)
|
XP_024308866.1:p.Gly32374Ala
|
|
XM_024453099.1:c.78884G>C
(TTN)
|
XP_024308867.1:p.Gly26295Ala
|
|
XM_024453100.1:c.68738G>C
(TTN)
|
XP_024308868.1:p.Gly22913Ala
|
|