ENST00000342992.11:c.51350T>C
(TTN)
|
ENSP00000343764.6:p.Val17117Ala
|
|
ENST00000342175.11:c.32435T>C
(TTN)
|
ENSP00000340554.6:p.Val10812Ala
|
|
ENST00000359218.10:c.32234T>C
(TTN)
|
ENSP00000352154.5:p.Val10745Ala
|
|
ENST00000342175.10:c.32435T>C
(TTN)
|
ENSP00000340554.6:p.Val10812Ala
|
|
ENST00000342992.10:c.51350T>C
(TTN)
|
ENSP00000343764.6:p.Val17117Ala
|
|
ENST00000359218.9:c.32234T>C
(TTN)
|
ENSP00000352154.5:p.Val10745Ala
|
|
ENST00000460472.6:c.31859T>C
(TTN)
|
ENSP00000434586.1:p.Val10620Ala
|
|
ENST00000589042.5:c.59054T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val19685Ala
|
|
ENST00000591111.5:c.54131T>C
(TTN)
|
ENSP00000465570.1:p.Val18044Ala
|
|
ENST00000615779.4:c.54131T>C
(TTN)
|
ENSP00000483597.1:p.Val18044Ala
|
|
NM_001256850.1:c.54131T>C
(TTN)
|
NP_001243779.1:p.Val18044Ala
|
|
NM_001267550.2:c.59054T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val19685Ala
|
|
NM_003319.4:c.31859T>C
(TTN)
|
NP_003310.4:p.Val10620Ala
|
|
NM_133378.4:c.51350T>C
(TTN)
|
NP_596869.4:p.Val17117Ala
|
|
NM_133432.3:c.32234T>C
(TTN)
|
NP_597676.3:p.Val10745Ala
|
|
NM_133437.4:c.32435T>C
(TTN)
|
NP_597681.4:p.Val10812Ala
|
|
NR_038271.1:n.597-4531A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1751A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.58151T>C
(TTN)
|
XP_011510031.1:p.Val19384Ala
|
|
XM_011511730.1:c.32045T>C
(TTN)
|
XP_011510032.1:p.Val10682Ala
|
|
XM_011511731.1:c.31904T>C
(TTN)
|
XP_011510033.1:p.Val10635Ala
|
|
XM_017004819.1:c.57947T>C
(TTN)
|
XP_016860308.1:p.Val19316Ala
|
|
XM_017004820.1:c.53345T>C
(TTN)
|
XP_016860309.1:p.Val17782Ala
|
|
XM_017004821.1:c.53342T>C
(TTN)
|
XP_016860310.1:p.Val17781Ala
|
|
XM_017004822.1:c.50384T>C
(TTN)
|
XP_016860311.1:p.Val16795Ala
|
|
XM_017004823.1:c.32000T>C
(TTN)
|
XP_016860312.1:p.Val10667Ala
|
|
XM_024453094.1:c.53495T>C
(TTN)
|
XP_024308862.1:p.Val17832Ala
|
|
XM_024453095.1:c.53492T>C
(TTN)
|
XP_024308863.1:p.Val17831Ala
|
|
XM_024453096.1:c.52925T>C
(TTN)
|
XP_024308864.1:p.Val17642Ala
|
|
XM_024453097.1:c.50267T>C
(TTN)
|
XP_024308865.1:p.Val16756Ala
|
|
XM_024453098.1:c.50186T>C
(TTN)
|
XP_024308866.1:p.Val16729Ala
|
|
XM_024453099.1:c.31949T>C
(TTN)
|
XP_024308867.1:p.Val10650Ala
|
|
XM_024453100.1:c.21803T>C
(TTN)
|
XP_024308868.1:p.Val7268Ala
|
|