ENST00000342992.11:c.41644C>G
(TTN)
|
ENSP00000343764.6:p.Pro13882Ala
|
|
ENST00000342175.11:c.22729C>G
(TTN)
|
ENSP00000340554.6:p.Pro7577Ala
|
|
ENST00000359218.10:c.22528C>G
(TTN)
|
ENSP00000352154.5:p.Pro7510Ala
|
|
ENST00000342175.10:c.22729C>G
(TTN)
|
ENSP00000340554.6:p.Pro7577Ala
|
|
ENST00000342992.10:c.41644C>G
(TTN)
|
ENSP00000343764.6:p.Pro13882Ala
|
|
ENST00000359218.9:c.22528C>G
(TTN)
|
ENSP00000352154.5:p.Pro7510Ala
|
|
ENST00000460472.6:c.22153C>G
(TTN)
|
ENSP00000434586.1:p.Pro7385Ala
|
|
ENST00000589042.5:c.49348C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro16450Ala
|
|
ENST00000591111.5:c.44425C>G
(TTN)
|
ENSP00000465570.1:p.Pro14809Ala
|
|
ENST00000615779.4:c.44425C>G
(TTN)
|
ENSP00000483597.1:p.Pro14809Ala
|
|
NM_001256850.1:c.44425C>G
(TTN)
|
NP_001243779.1:p.Pro14809Ala
|
|
NM_001267550.2:c.49348C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro16450Ala
|
|
NM_003319.4:c.22153C>G
(TTN)
|
NP_003310.4:p.Pro7385Ala
|
|
NM_133378.4:c.41644C>G
(TTN)
|
NP_596869.4:p.Pro13882Ala
|
|
NM_133432.3:c.22528C>G
(TTN)
|
NP_597676.3:p.Pro7510Ala
|
|
NM_133437.4:c.22729C>G
(TTN)
|
NP_597681.4:p.Pro7577Ala
|
|
NR_038271.1:n.783-100G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.48445C>G
(TTN)
|
XP_011510031.1:p.Pro16149Ala
|
|
XM_011511730.1:c.22339C>G
(TTN)
|
XP_011510032.1:p.Pro7447Ala
|
|
XM_011511731.1:c.22198C>G
(TTN)
|
XP_011510033.1:p.Pro7400Ala
|
|
XM_017004819.1:c.48241C>G
(TTN)
|
XP_016860308.1:p.Pro16081Ala
|
|
XM_017004820.1:c.43639C>G
(TTN)
|
XP_016860309.1:p.Pro14547Ala
|
|
XM_017004821.1:c.43636C>G
(TTN)
|
XP_016860310.1:p.Pro14546Ala
|
|
XM_017004822.1:c.40678C>G
(TTN)
|
XP_016860311.1:p.Pro13560Ala
|
|
XM_017004823.1:c.22294C>G
(TTN)
|
XP_016860312.1:p.Pro7432Ala
|
|
XM_024453094.1:c.43789C>G
(TTN)
|
XP_024308862.1:p.Pro14597Ala
|
|
XM_024453095.1:c.43786C>G
(TTN)
|
XP_024308863.1:p.Pro14596Ala
|
|
XM_024453096.1:c.43219C>G
(TTN)
|
XP_024308864.1:p.Pro14407Ala
|
|
XM_024453097.1:c.40561C>G
(TTN)
|
XP_024308865.1:p.Pro13521Ala
|
|
XM_024453098.1:c.40480C>G
(TTN)
|
XP_024308866.1:p.Pro13494Ala
|
|
XM_024453099.1:c.22243C>G
(TTN)
|
XP_024308867.1:p.Pro7415Ala
|
|
XM_024453100.1:c.12097C>G
(TTN)
|
XP_024308868.1:p.Pro4033Ala
|
|