ENST00000342992.11:c.91876C>G
(TTN)
|
ENSP00000343764.6:p.Pro30626Ala
|
|
ENST00000342175.11:c.72961C>G
(TTN)
|
ENSP00000340554.6:p.Pro24321Ala
|
|
ENST00000359218.10:c.72760C>G
(TTN)
|
ENSP00000352154.5:p.Pro24254Ala
|
|
ENST00000342175.10:c.72961C>G
(TTN)
|
ENSP00000340554.6:p.Pro24321Ala
|
|
ENST00000342992.10:c.91876C>G
(TTN)
|
ENSP00000343764.6:p.Pro30626Ala
|
|
ENST00000359218.9:c.72760C>G
(TTN)
|
ENSP00000352154.5:p.Pro24254Ala
|
|
ENST00000460472.6:c.72385C>G
(TTN)
|
ENSP00000434586.1:p.Pro24129Ala
|
|
ENST00000589042.5:c.99580C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro33194Ala
|
|
ENST00000591111.5:c.94657C>G
(TTN)
|
ENSP00000465570.1:p.Pro31553Ala
|
|
ENST00000615779.4:c.94657C>G
(TTN)
|
ENSP00000483597.1:p.Pro31553Ala
|
|
NM_001256850.1:c.94657C>G
(TTN)
|
NP_001243779.1:p.Pro31553Ala
|
|
NM_001267550.2:c.99580C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro33194Ala
|
|
NM_003319.4:c.72385C>G
(TTN)
|
NP_003310.4:p.Pro24129Ala
|
|
NM_133378.4:c.91876C>G
(TTN)
|
NP_596869.4:p.Pro30626Ala
|
|
NM_133432.3:c.72760C>G
(TTN)
|
NP_597676.3:p.Pro24254Ala
|
|
NM_133437.4:c.72961C>G
(TTN)
|
NP_597681.4:p.Pro24321Ala
|
|
NR_038271.1:n.446+13991G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.583G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.98677C>G
(TTN)
|
XP_011510031.1:p.Pro32893Ala
|
|
XM_011511730.1:c.72571C>G
(TTN)
|
XP_011510032.1:p.Pro24191Ala
|
|
XM_011511731.1:c.72430C>G
(TTN)
|
XP_011510033.1:p.Pro24144Ala
|
|
XM_017004819.1:c.98473C>G
(TTN)
|
XP_016860308.1:p.Pro32825Ala
|
|
XM_017004820.1:c.93871C>G
(TTN)
|
XP_016860309.1:p.Pro31291Ala
|
|
XM_017004821.1:c.93868C>G
(TTN)
|
XP_016860310.1:p.Pro31290Ala
|
|
XM_017004822.1:c.90910C>G
(TTN)
|
XP_016860311.1:p.Pro30304Ala
|
|
XM_017004823.1:c.72526C>G
(TTN)
|
XP_016860312.1:p.Pro24176Ala
|
|
XM_024453094.1:c.94021C>G
(TTN)
|
XP_024308862.1:p.Pro31341Ala
|
|
XM_024453095.1:c.94018C>G
(TTN)
|
XP_024308863.1:p.Pro31340Ala
|
|
XM_024453096.1:c.93451C>G
(TTN)
|
XP_024308864.1:p.Pro31151Ala
|
|
XM_024453097.1:c.90793C>G
(TTN)
|
XP_024308865.1:p.Pro30265Ala
|
|
XM_024453098.1:c.90712C>G
(TTN)
|
XP_024308866.1:p.Pro30238Ala
|
|
XM_024453099.1:c.72475C>G
(TTN)
|
XP_024308867.1:p.Pro24159Ala
|
|
XM_024453100.1:c.62329C>G
(TTN)
|
XP_024308868.1:p.Pro20777Ala
|
|