ENST00000342992.11:c.88126T>C
(TTN)
|
ENSP00000343764.6:p.Tyr29376His
|
|
ENST00000342175.11:c.69211T>C
(TTN)
|
ENSP00000340554.6:p.Tyr23071His
|
|
ENST00000359218.10:c.69010T>C
(TTN)
|
ENSP00000352154.5:p.Tyr23004His
|
|
ENST00000342175.10:c.69211T>C
(TTN)
|
ENSP00000340554.6:p.Tyr23071His
|
|
ENST00000342992.10:c.88126T>C
(TTN)
|
ENSP00000343764.6:p.Tyr29376His
|
|
ENST00000359218.9:c.69010T>C
(TTN)
|
ENSP00000352154.5:p.Tyr23004His
|
|
ENST00000460472.6:c.68635T>C
(TTN)
|
ENSP00000434586.1:p.Tyr22879His
|
|
ENST00000589042.5:c.95830T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr31944His
|
|
ENST00000591111.5:c.90907T>C
(TTN)
|
ENSP00000465570.1:p.Tyr30303His
|
|
ENST00000615779.4:c.90907T>C
(TTN)
|
ENSP00000483597.1:p.Tyr30303His
|
|
NM_001256850.1:c.90907T>C
(TTN)
|
NP_001243779.1:p.Tyr30303His
|
|
NM_001267550.2:c.95830T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr31944His
|
|
NM_003319.4:c.68635T>C
(TTN)
|
NP_003310.4:p.Tyr22879His
|
|
NM_133378.4:c.88126T>C
(TTN)
|
NP_596869.4:p.Tyr29376His
|
|
NM_133432.3:c.69010T>C
(TTN)
|
NP_597676.3:p.Tyr23004His
|
|
NM_133437.4:c.69211T>C
(TTN)
|
NP_597681.4:p.Tyr23071His
|
|
NR_038271.1:n.446+20763A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2038A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.94927T>C
(TTN)
|
XP_011510031.1:p.Tyr31643His
|
|
XM_011511730.1:c.68821T>C
(TTN)
|
XP_011510032.1:p.Tyr22941His
|
|
XM_011511731.1:c.68680T>C
(TTN)
|
XP_011510033.1:p.Tyr22894His
|
|
XM_017004819.1:c.94723T>C
(TTN)
|
XP_016860308.1:p.Tyr31575His
|
|
XM_017004820.1:c.90121T>C
(TTN)
|
XP_016860309.1:p.Tyr30041His
|
|
XM_017004821.1:c.90118T>C
(TTN)
|
XP_016860310.1:p.Tyr30040His
|
|
XM_017004822.1:c.87160T>C
(TTN)
|
XP_016860311.1:p.Tyr29054His
|
|
XM_017004823.1:c.68776T>C
(TTN)
|
XP_016860312.1:p.Tyr22926His
|
|
XM_024453094.1:c.90271T>C
(TTN)
|
XP_024308862.1:p.Tyr30091His
|
|
XM_024453095.1:c.90268T>C
(TTN)
|
XP_024308863.1:p.Tyr30090His
|
|
XM_024453096.1:c.89701T>C
(TTN)
|
XP_024308864.1:p.Tyr29901His
|
|
XM_024453097.1:c.87043T>C
(TTN)
|
XP_024308865.1:p.Tyr29015His
|
|
XM_024453098.1:c.86962T>C
(TTN)
|
XP_024308866.1:p.Tyr28988His
|
|
XM_024453099.1:c.68725T>C
(TTN)
|
XP_024308867.1:p.Tyr22909His
|
|
XM_024453100.1:c.58579T>C
(TTN)
|
XP_024308868.1:p.Tyr19527His
|
|