ENST00000342992.11:c.98406C>T
(TTN)
|
ENSP00000343764.6:p.Thr32802=
|
|
ENST00000342175.11:c.79491C>T
(TTN)
|
ENSP00000340554.6:p.Thr26497=
|
|
ENST00000359218.10:c.79290C>T
(TTN)
|
ENSP00000352154.5:p.Thr26430=
|
|
ENST00000342175.10:c.79491C>T
(TTN)
|
ENSP00000340554.6:p.Thr26497=
|
|
ENST00000342992.10:c.98406C>T
(TTN)
|
ENSP00000343764.6:p.Thr32802=
|
|
ENST00000359218.9:c.79290C>T
(TTN)
|
ENSP00000352154.5:p.Thr26430=
|
|
ENST00000460472.6:c.78915C>T
(TTN)
|
ENSP00000434586.1:p.Thr26305=
|
|
ENST00000589042.5:c.106110C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35370=
|
|
ENST00000591111.5:c.101187C>T
(TTN)
|
ENSP00000465570.1:p.Thr33729=
|
|
ENST00000615779.4:c.101187C>T
(TTN)
|
ENSP00000483597.1:p.Thr33729=
|
|
NM_001256850.1:c.101187C>T
(TTN)
|
NP_001243779.1:p.Thr33729=
|
|
NM_001267550.2:c.106110C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35370=
|
|
NM_003319.4:c.78915C>T
(TTN)
|
NP_003310.4:p.Thr26305=
|
|
NM_133378.4:c.98406C>T
(TTN)
|
NP_596869.4:p.Thr32802=
|
|
NM_133432.3:c.79290C>T
(TTN)
|
NP_597676.3:p.Thr26430=
|
|
NM_133437.4:c.79491C>T
(TTN)
|
NP_597681.4:p.Thr26497=
|
|
NR_038271.1:n.446+6869G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5227G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105207C>T
(TTN)
|
XP_011510031.1:p.Thr35069=
|
|
XM_011511730.1:c.79101C>T
(TTN)
|
XP_011510032.1:p.Thr26367=
|
|
XM_011511731.1:c.78960C>T
(TTN)
|
XP_011510033.1:p.Thr26320=
|
|
XM_017004819.1:c.105003C>T
(TTN)
|
XP_016860308.1:p.Thr35001=
|
|
XM_017004820.1:c.100401C>T
(TTN)
|
XP_016860309.1:p.Thr33467=
|
|
XM_017004821.1:c.100398C>T
(TTN)
|
XP_016860310.1:p.Thr33466=
|
|
XM_017004822.1:c.97440C>T
(TTN)
|
XP_016860311.1:p.Thr32480=
|
|
XM_017004823.1:c.79056C>T
(TTN)
|
XP_016860312.1:p.Thr26352=
|
|
XM_024453094.1:c.100551C>T
(TTN)
|
XP_024308862.1:p.Thr33517=
|
|
XM_024453095.1:c.100548C>T
(TTN)
|
XP_024308863.1:p.Thr33516=
|
|
XM_024453096.1:c.99981C>T
(TTN)
|
XP_024308864.1:p.Thr33327=
|
|
XM_024453097.1:c.97323C>T
(TTN)
|
XP_024308865.1:p.Thr32441=
|
|
XM_024453098.1:c.97242C>T
(TTN)
|
XP_024308866.1:p.Thr32414=
|
|
XM_024453099.1:c.79005C>T
(TTN)
|
XP_024308867.1:p.Thr26335=
|
|
XM_024453100.1:c.68859C>T
(TTN)
|
XP_024308868.1:p.Thr22953=
|
|