ENST00000342992.11:c.98595A>G
(TTN)
|
ENSP00000343764.6:p.Ser32865=
|
|
ENST00000342175.11:c.79680A>G
(TTN)
|
ENSP00000340554.6:p.Ser26560=
|
|
ENST00000359218.10:c.79479A>G
(TTN)
|
ENSP00000352154.5:p.Ser26493=
|
|
ENST00000342175.10:c.79680A>G
(TTN)
|
ENSP00000340554.6:p.Ser26560=
|
|
ENST00000342992.10:c.98595A>G
(TTN)
|
ENSP00000343764.6:p.Ser32865=
|
|
ENST00000359218.9:c.79479A>G
(TTN)
|
ENSP00000352154.5:p.Ser26493=
|
|
ENST00000460472.6:c.79104A>G
(TTN)
|
ENSP00000434586.1:p.Ser26368=
|
|
ENST00000589042.5:c.106299A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35433=
|
|
ENST00000591111.5:c.101376A>G
(TTN)
|
ENSP00000465570.1:p.Ser33792=
|
|
ENST00000615779.4:c.101376A>G
(TTN)
|
ENSP00000483597.1:p.Ser33792=
|
|
NM_001256850.1:c.101376A>G
(TTN)
|
NP_001243779.1:p.Ser33792=
|
|
NM_001267550.2:c.106299A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35433=
|
|
NM_003319.4:c.79104A>G
(TTN)
|
NP_003310.4:p.Ser26368=
|
|
NM_133378.4:c.98595A>G
(TTN)
|
NP_596869.4:p.Ser32865=
|
|
NM_133432.3:c.79479A>G
(TTN)
|
NP_597676.3:p.Ser26493=
|
|
NM_133437.4:c.79680A>G
(TTN)
|
NP_597681.4:p.Ser26560=
|
|
NR_038271.1:n.446+6680T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5416T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105396A>G
(TTN)
|
XP_011510031.1:p.Ser35132=
|
|
XM_011511730.1:c.79290A>G
(TTN)
|
XP_011510032.1:p.Ser26430=
|
|
XM_011511731.1:c.79149A>G
(TTN)
|
XP_011510033.1:p.Ser26383=
|
|
XM_017004819.1:c.105192A>G
(TTN)
|
XP_016860308.1:p.Ser35064=
|
|
XM_017004820.1:c.100590A>G
(TTN)
|
XP_016860309.1:p.Ser33530=
|
|
XM_017004821.1:c.100587A>G
(TTN)
|
XP_016860310.1:p.Ser33529=
|
|
XM_017004822.1:c.97629A>G
(TTN)
|
XP_016860311.1:p.Ser32543=
|
|
XM_017004823.1:c.79245A>G
(TTN)
|
XP_016860312.1:p.Ser26415=
|
|
XM_024453094.1:c.100740A>G
(TTN)
|
XP_024308862.1:p.Ser33580=
|
|
XM_024453095.1:c.100737A>G
(TTN)
|
XP_024308863.1:p.Ser33579=
|
|
XM_024453096.1:c.100170A>G
(TTN)
|
XP_024308864.1:p.Ser33390=
|
|
XM_024453097.1:c.97512A>G
(TTN)
|
XP_024308865.1:p.Ser32504=
|
|
XM_024453098.1:c.97431A>G
(TTN)
|
XP_024308866.1:p.Ser32477=
|
|
XM_024453099.1:c.79194A>G
(TTN)
|
XP_024308867.1:p.Ser26398=
|
|
XM_024453100.1:c.69048A>G
(TTN)
|
XP_024308868.1:p.Ser23016=
|
|