ENST00000342992.11:c.98264G>C
(TTN)
|
ENSP00000343764.6:p.Gly32755Ala
|
|
ENST00000342175.11:c.79349G>C
(TTN)
|
ENSP00000340554.6:p.Gly26450Ala
|
|
ENST00000359218.10:c.79148G>C
(TTN)
|
ENSP00000352154.5:p.Gly26383Ala
|
|
ENST00000342175.10:c.79349G>C
(TTN)
|
ENSP00000340554.6:p.Gly26450Ala
|
|
ENST00000342992.10:c.98264G>C
(TTN)
|
ENSP00000343764.6:p.Gly32755Ala
|
|
ENST00000359218.9:c.79148G>C
(TTN)
|
ENSP00000352154.5:p.Gly26383Ala
|
|
ENST00000460472.6:c.78773G>C
(TTN)
|
ENSP00000434586.1:p.Gly26258Ala
|
|
ENST00000589042.5:c.105968G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35323Ala
|
|
ENST00000591111.5:c.101045G>C
(TTN)
|
ENSP00000465570.1:p.Gly33682Ala
|
|
ENST00000615779.4:c.101045G>C
(TTN)
|
ENSP00000483597.1:p.Gly33682Ala
|
|
NM_001256850.1:c.101045G>C
(TTN)
|
NP_001243779.1:p.Gly33682Ala
|
|
NM_001267550.2:c.105968G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35323Ala
|
|
NM_003319.4:c.78773G>C
(TTN)
|
NP_003310.4:p.Gly26258Ala
|
|
NM_133378.4:c.98264G>C
(TTN)
|
NP_596869.4:p.Gly32755Ala
|
|
NM_133432.3:c.79148G>C
(TTN)
|
NP_597676.3:p.Gly26383Ala
|
|
NM_133437.4:c.79349G>C
(TTN)
|
NP_597681.4:p.Gly26450Ala
|
|
NR_038271.1:n.446+7011C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5085C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105065G>C
(TTN)
|
XP_011510031.1:p.Gly35022Ala
|
|
XM_011511730.1:c.78959G>C
(TTN)
|
XP_011510032.1:p.Gly26320Ala
|
|
XM_011511731.1:c.78818G>C
(TTN)
|
XP_011510033.1:p.Gly26273Ala
|
|
XM_017004819.1:c.104861G>C
(TTN)
|
XP_016860308.1:p.Gly34954Ala
|
|
XM_017004820.1:c.100259G>C
(TTN)
|
XP_016860309.1:p.Gly33420Ala
|
|
XM_017004821.1:c.100256G>C
(TTN)
|
XP_016860310.1:p.Gly33419Ala
|
|
XM_017004822.1:c.97298G>C
(TTN)
|
XP_016860311.1:p.Gly32433Ala
|
|
XM_017004823.1:c.78914G>C
(TTN)
|
XP_016860312.1:p.Gly26305Ala
|
|
XM_024453094.1:c.100409G>C
(TTN)
|
XP_024308862.1:p.Gly33470Ala
|
|
XM_024453095.1:c.100406G>C
(TTN)
|
XP_024308863.1:p.Gly33469Ala
|
|
XM_024453096.1:c.99839G>C
(TTN)
|
XP_024308864.1:p.Gly33280Ala
|
|
XM_024453097.1:c.97181G>C
(TTN)
|
XP_024308865.1:p.Gly32394Ala
|
|
XM_024453098.1:c.97100G>C
(TTN)
|
XP_024308866.1:p.Gly32367Ala
|
|
XM_024453099.1:c.78863G>C
(TTN)
|
XP_024308867.1:p.Gly26288Ala
|
|
XM_024453100.1:c.68717G>C
(TTN)
|
XP_024308868.1:p.Gly22906Ala
|
|