ENST00000342992.11:c.98328C>G
(TTN)
|
ENSP00000343764.6:p.Leu32776=
|
|
ENST00000342175.11:c.79413C>G
(TTN)
|
ENSP00000340554.6:p.Leu26471=
|
|
ENST00000359218.10:c.79212C>G
(TTN)
|
ENSP00000352154.5:p.Leu26404=
|
|
ENST00000342175.10:c.79413C>G
(TTN)
|
ENSP00000340554.6:p.Leu26471=
|
|
ENST00000342992.10:c.98328C>G
(TTN)
|
ENSP00000343764.6:p.Leu32776=
|
|
ENST00000359218.9:c.79212C>G
(TTN)
|
ENSP00000352154.5:p.Leu26404=
|
|
ENST00000460472.6:c.78837C>G
(TTN)
|
ENSP00000434586.1:p.Leu26279=
|
|
ENST00000589042.5:c.106032C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35344=
|
|
ENST00000591111.5:c.101109C>G
(TTN)
|
ENSP00000465570.1:p.Leu33703=
|
|
ENST00000615779.4:c.101109C>G
(TTN)
|
ENSP00000483597.1:p.Leu33703=
|
|
NM_001256850.1:c.101109C>G
(TTN)
|
NP_001243779.1:p.Leu33703=
|
|
NM_001267550.2:c.106032C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35344=
|
|
NM_003319.4:c.78837C>G
(TTN)
|
NP_003310.4:p.Leu26279=
|
|
NM_133378.4:c.98328C>G
(TTN)
|
NP_596869.4:p.Leu32776=
|
|
NM_133432.3:c.79212C>G
(TTN)
|
NP_597676.3:p.Leu26404=
|
|
NM_133437.4:c.79413C>G
(TTN)
|
NP_597681.4:p.Leu26471=
|
|
NR_038271.1:n.446+6947G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5149G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105129C>G
(TTN)
|
XP_011510031.1:p.Leu35043=
|
|
XM_011511730.1:c.79023C>G
(TTN)
|
XP_011510032.1:p.Leu26341=
|
|
XM_011511731.1:c.78882C>G
(TTN)
|
XP_011510033.1:p.Leu26294=
|
|
XM_017004819.1:c.104925C>G
(TTN)
|
XP_016860308.1:p.Leu34975=
|
|
XM_017004820.1:c.100323C>G
(TTN)
|
XP_016860309.1:p.Leu33441=
|
|
XM_017004821.1:c.100320C>G
(TTN)
|
XP_016860310.1:p.Leu33440=
|
|
XM_017004822.1:c.97362C>G
(TTN)
|
XP_016860311.1:p.Leu32454=
|
|
XM_017004823.1:c.78978C>G
(TTN)
|
XP_016860312.1:p.Leu26326=
|
|
XM_024453094.1:c.100473C>G
(TTN)
|
XP_024308862.1:p.Leu33491=
|
|
XM_024453095.1:c.100470C>G
(TTN)
|
XP_024308863.1:p.Leu33490=
|
|
XM_024453096.1:c.99903C>G
(TTN)
|
XP_024308864.1:p.Leu33301=
|
|
XM_024453097.1:c.97245C>G
(TTN)
|
XP_024308865.1:p.Leu32415=
|
|
XM_024453098.1:c.97164C>G
(TTN)
|
XP_024308866.1:p.Leu32388=
|
|
XM_024453099.1:c.78927C>G
(TTN)
|
XP_024308867.1:p.Leu26309=
|
|
XM_024453100.1:c.68781C>G
(TTN)
|
XP_024308868.1:p.Leu22927=
|
|