ENST00000342992.11:c.63633C>T
(TTN)
|
ENSP00000343764.6:p.Thr21211=
|
|
ENST00000342175.11:c.44718C>T
(TTN)
|
ENSP00000340554.6:p.Thr14906=
|
|
ENST00000359218.10:c.44517C>T
(TTN)
|
ENSP00000352154.5:p.Thr14839=
|
|
ENST00000342175.10:c.44718C>T
(TTN)
|
ENSP00000340554.6:p.Thr14906=
|
|
ENST00000342992.10:c.63633C>T
(TTN)
|
ENSP00000343764.6:p.Thr21211=
|
|
ENST00000359218.9:c.44517C>T
(TTN)
|
ENSP00000352154.5:p.Thr14839=
|
|
ENST00000460472.6:c.44142C>T
(TTN)
|
ENSP00000434586.1:p.Thr14714=
|
|
ENST00000589042.5:c.71337C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr23779=
|
|
ENST00000591111.5:c.66414C>T
(TTN)
|
ENSP00000465570.1:p.Thr22138=
|
|
ENST00000615779.4:c.66414C>T
(TTN)
|
ENSP00000483597.1:p.Thr22138=
|
|
NM_001256850.1:c.66414C>T
(TTN)
|
NP_001243779.1:p.Thr22138=
|
|
NM_001267550.2:c.71337C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr23779=
|
|
NM_003319.4:c.44142C>T
(TTN)
|
NP_003310.4:p.Thr14714=
|
|
NM_133378.4:c.63633C>T
(TTN)
|
NP_596869.4:p.Thr21211=
|
|
NM_133432.3:c.44517C>T
(TTN)
|
NP_597676.3:p.Thr14839=
|
|
NM_133437.4:c.44718C>T
(TTN)
|
NP_597681.4:p.Thr14906=
|
|
NR_038271.1:n.596+3346G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7777G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.70434C>T
(TTN)
|
XP_011510031.1:p.Thr23478=
|
|
XM_011511730.1:c.44328C>T
(TTN)
|
XP_011510032.1:p.Thr14776=
|
|
XM_011511731.1:c.44187C>T
(TTN)
|
XP_011510033.1:p.Thr14729=
|
|
XM_017004819.1:c.70230C>T
(TTN)
|
XP_016860308.1:p.Thr23410=
|
|
XM_017004820.1:c.65628C>T
(TTN)
|
XP_016860309.1:p.Thr21876=
|
|
XM_017004821.1:c.65625C>T
(TTN)
|
XP_016860310.1:p.Thr21875=
|
|
XM_017004822.1:c.62667C>T
(TTN)
|
XP_016860311.1:p.Thr20889=
|
|
XM_017004823.1:c.44283C>T
(TTN)
|
XP_016860312.1:p.Thr14761=
|
|
XM_024453094.1:c.65778C>T
(TTN)
|
XP_024308862.1:p.Thr21926=
|
|
XM_024453095.1:c.65775C>T
(TTN)
|
XP_024308863.1:p.Thr21925=
|
|
XM_024453096.1:c.65208C>T
(TTN)
|
XP_024308864.1:p.Thr21736=
|
|
XM_024453097.1:c.62550C>T
(TTN)
|
XP_024308865.1:p.Thr20850=
|
|
XM_024453098.1:c.62469C>T
(TTN)
|
XP_024308866.1:p.Thr20823=
|
|
XM_024453099.1:c.44232C>T
(TTN)
|
XP_024308867.1:p.Thr14744=
|
|
XM_024453100.1:c.34086C>T
(TTN)
|
XP_024308868.1:p.Thr11362=
|
|