ENST00000342992.11:c.98265C>G
(TTN)
|
ENSP00000343764.6:p.Gly32755=
|
|
ENST00000342175.11:c.79350C>G
(TTN)
|
ENSP00000340554.6:p.Gly26450=
|
|
ENST00000359218.10:c.79149C>G
(TTN)
|
ENSP00000352154.5:p.Gly26383=
|
|
ENST00000342175.10:c.79350C>G
(TTN)
|
ENSP00000340554.6:p.Gly26450=
|
|
ENST00000342992.10:c.98265C>G
(TTN)
|
ENSP00000343764.6:p.Gly32755=
|
|
ENST00000359218.9:c.79149C>G
(TTN)
|
ENSP00000352154.5:p.Gly26383=
|
|
ENST00000460472.6:c.78774C>G
(TTN)
|
ENSP00000434586.1:p.Gly26258=
|
|
ENST00000589042.5:c.105969C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35323=
|
|
ENST00000591111.5:c.101046C>G
(TTN)
|
ENSP00000465570.1:p.Gly33682=
|
|
ENST00000615779.4:c.101046C>G
(TTN)
|
ENSP00000483597.1:p.Gly33682=
|
|
NM_001256850.1:c.101046C>G
(TTN)
|
NP_001243779.1:p.Gly33682=
|
|
NM_001267550.2:c.105969C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35323=
|
|
NM_003319.4:c.78774C>G
(TTN)
|
NP_003310.4:p.Gly26258=
|
|
NM_133378.4:c.98265C>G
(TTN)
|
NP_596869.4:p.Gly32755=
|
|
NM_133432.3:c.79149C>G
(TTN)
|
NP_597676.3:p.Gly26383=
|
|
NM_133437.4:c.79350C>G
(TTN)
|
NP_597681.4:p.Gly26450=
|
|
NR_038271.1:n.446+7010G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5086G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105066C>G
(TTN)
|
XP_011510031.1:p.Gly35022=
|
|
XM_011511730.1:c.78960C>G
(TTN)
|
XP_011510032.1:p.Gly26320=
|
|
XM_011511731.1:c.78819C>G
(TTN)
|
XP_011510033.1:p.Gly26273=
|
|
XM_017004819.1:c.104862C>G
(TTN)
|
XP_016860308.1:p.Gly34954=
|
|
XM_017004820.1:c.100260C>G
(TTN)
|
XP_016860309.1:p.Gly33420=
|
|
XM_017004821.1:c.100257C>G
(TTN)
|
XP_016860310.1:p.Gly33419=
|
|
XM_017004822.1:c.97299C>G
(TTN)
|
XP_016860311.1:p.Gly32433=
|
|
XM_017004823.1:c.78915C>G
(TTN)
|
XP_016860312.1:p.Gly26305=
|
|
XM_024453094.1:c.100410C>G
(TTN)
|
XP_024308862.1:p.Gly33470=
|
|
XM_024453095.1:c.100407C>G
(TTN)
|
XP_024308863.1:p.Gly33469=
|
|
XM_024453096.1:c.99840C>G
(TTN)
|
XP_024308864.1:p.Gly33280=
|
|
XM_024453097.1:c.97182C>G
(TTN)
|
XP_024308865.1:p.Gly32394=
|
|
XM_024453098.1:c.97101C>G
(TTN)
|
XP_024308866.1:p.Gly32367=
|
|
XM_024453099.1:c.78864C>G
(TTN)
|
XP_024308867.1:p.Gly26288=
|
|
XM_024453100.1:c.68718C>G
(TTN)
|
XP_024308868.1:p.Gly22906=
|
|