ENST00000342992.11:c.96664C>T
(TTN)
|
ENSP00000343764.6:p.Leu32222Phe
|
|
ENST00000342175.11:c.77749C>T
(TTN)
|
ENSP00000340554.6:p.Leu25917Phe
|
|
ENST00000359218.10:c.77548C>T
(TTN)
|
ENSP00000352154.5:p.Leu25850Phe
|
|
ENST00000342175.10:c.77749C>T
(TTN)
|
ENSP00000340554.6:p.Leu25917Phe
|
|
ENST00000342992.10:c.96664C>T
(TTN)
|
ENSP00000343764.6:p.Leu32222Phe
|
|
ENST00000359218.9:c.77548C>T
(TTN)
|
ENSP00000352154.5:p.Leu25850Phe
|
|
ENST00000460472.6:c.77173C>T
(TTN)
|
ENSP00000434586.1:p.Leu25725Phe
|
|
ENST00000589042.5:c.104368C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34790Phe
|
|
ENST00000591111.5:c.99445C>T
(TTN)
|
ENSP00000465570.1:p.Leu33149Phe
|
|
ENST00000615779.4:c.99445C>T
(TTN)
|
ENSP00000483597.1:p.Leu33149Phe
|
|
NM_001256850.1:c.99445C>T
(TTN)
|
NP_001243779.1:p.Leu33149Phe
|
|
NM_001267550.2:c.104368C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34790Phe
|
|
NM_003319.4:c.77173C>T
(TTN)
|
NP_003310.4:p.Leu25725Phe
|
|
NM_133378.4:c.96664C>T
(TTN)
|
NP_596869.4:p.Leu32222Phe
|
|
NM_133432.3:c.77548C>T
(TTN)
|
NP_597676.3:p.Leu25850Phe
|
|
NM_133437.4:c.77749C>T
(TTN)
|
NP_597681.4:p.Leu25917Phe
|
|
NR_038271.1:n.446+8611G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3485G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103465C>T
(TTN)
|
XP_011510031.1:p.Leu34489Phe
|
|
XM_011511730.1:c.77359C>T
(TTN)
|
XP_011510032.1:p.Leu25787Phe
|
|
XM_011511731.1:c.77218C>T
(TTN)
|
XP_011510033.1:p.Leu25740Phe
|
|
XM_017004819.1:c.103261C>T
(TTN)
|
XP_016860308.1:p.Leu34421Phe
|
|
XM_017004820.1:c.98659C>T
(TTN)
|
XP_016860309.1:p.Leu32887Phe
|
|
XM_017004821.1:c.98656C>T
(TTN)
|
XP_016860310.1:p.Leu32886Phe
|
|
XM_017004822.1:c.95698C>T
(TTN)
|
XP_016860311.1:p.Leu31900Phe
|
|
XM_017004823.1:c.77314C>T
(TTN)
|
XP_016860312.1:p.Leu25772Phe
|
|
XM_024453094.1:c.98809C>T
(TTN)
|
XP_024308862.1:p.Leu32937Phe
|
|
XM_024453095.1:c.98806C>T
(TTN)
|
XP_024308863.1:p.Leu32936Phe
|
|
XM_024453096.1:c.98239C>T
(TTN)
|
XP_024308864.1:p.Leu32747Phe
|
|
XM_024453097.1:c.95581C>T
(TTN)
|
XP_024308865.1:p.Leu31861Phe
|
|
XM_024453098.1:c.95500C>T
(TTN)
|
XP_024308866.1:p.Leu31834Phe
|
|
XM_024453099.1:c.77263C>T
(TTN)
|
XP_024308867.1:p.Leu25755Phe
|
|
XM_024453100.1:c.67117C>T
(TTN)
|
XP_024308868.1:p.Leu22373Phe
|
|