ENST00000342992.11:c.47346A>G
(TTN)
|
ENSP00000343764.6:p.Lys15782=
|
|
ENST00000342175.11:c.28431A>G
(TTN)
|
ENSP00000340554.6:p.Lys9477=
|
|
ENST00000359218.10:c.28230A>G
(TTN)
|
ENSP00000352154.5:p.Lys9410=
|
|
ENST00000342175.10:c.28431A>G
(TTN)
|
ENSP00000340554.6:p.Lys9477=
|
|
ENST00000342992.10:c.47346A>G
(TTN)
|
ENSP00000343764.6:p.Lys15782=
|
|
ENST00000359218.9:c.28230A>G
(TTN)
|
ENSP00000352154.5:p.Lys9410=
|
|
ENST00000460472.6:c.27855A>G
(TTN)
|
ENSP00000434586.1:p.Lys9285=
|
|
ENST00000589042.5:c.55050A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys18350=
|
|
ENST00000591111.5:c.50127A>G
(TTN)
|
ENSP00000465570.1:p.Lys16709=
|
|
ENST00000615779.4:c.50127A>G
(TTN)
|
ENSP00000483597.1:p.Lys16709=
|
|
NM_001256850.1:c.50127A>G
(TTN)
|
NP_001243779.1:p.Lys16709=
|
|
NM_001267550.2:c.55050A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Lys18350=
|
|
NM_003319.4:c.27855A>G
(TTN)
|
NP_003310.4:p.Lys9285=
|
|
NM_133378.4:c.47346A>G
(TTN)
|
NP_596869.4:p.Lys15782=
|
|
NM_133432.3:c.28230A>G
(TTN)
|
NP_597676.3:p.Lys9410=
|
|
NM_133437.4:c.28431A>G
(TTN)
|
NP_597681.4:p.Lys9477=
|
|
NR_038271.1:n.682+4671T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1685T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.54147A>G
(TTN)
|
XP_011510031.1:p.Lys18049=
|
|
XM_011511730.1:c.28041A>G
(TTN)
|
XP_011510032.1:p.Lys9347=
|
|
XM_011511731.1:c.27900A>G
(TTN)
|
XP_011510033.1:p.Lys9300=
|
|
XM_017004819.1:c.53943A>G
(TTN)
|
XP_016860308.1:p.Lys17981=
|
|
XM_017004820.1:c.49341A>G
(TTN)
|
XP_016860309.1:p.Lys16447=
|
|
XM_017004821.1:c.49338A>G
(TTN)
|
XP_016860310.1:p.Lys16446=
|
|
XM_017004822.1:c.46380A>G
(TTN)
|
XP_016860311.1:p.Lys15460=
|
|
XM_017004823.1:c.27996A>G
(TTN)
|
XP_016860312.1:p.Lys9332=
|
|
XM_024453094.1:c.49491A>G
(TTN)
|
XP_024308862.1:p.Lys16497=
|
|
XM_024453095.1:c.49488A>G
(TTN)
|
XP_024308863.1:p.Lys16496=
|
|
XM_024453096.1:c.48921A>G
(TTN)
|
XP_024308864.1:p.Lys16307=
|
|
XM_024453097.1:c.46263A>G
(TTN)
|
XP_024308865.1:p.Lys15421=
|
|
XM_024453098.1:c.46182A>G
(TTN)
|
XP_024308866.1:p.Lys15394=
|
|
XM_024453099.1:c.27945A>G
(TTN)
|
XP_024308867.1:p.Lys9315=
|
|
XM_024453100.1:c.17799A>G
(TTN)
|
XP_024308868.1:p.Lys5933=
|
|