ENST00000342992.11:c.96807G>T
(TTN)
|
ENSP00000343764.6:p.Leu32269=
|
|
ENST00000342175.11:c.77892G>T
(TTN)
|
ENSP00000340554.6:p.Leu25964=
|
|
ENST00000359218.10:c.77691G>T
(TTN)
|
ENSP00000352154.5:p.Leu25897=
|
|
ENST00000342175.10:c.77892G>T
(TTN)
|
ENSP00000340554.6:p.Leu25964=
|
|
ENST00000342992.10:c.96807G>T
(TTN)
|
ENSP00000343764.6:p.Leu32269=
|
|
ENST00000359218.9:c.77691G>T
(TTN)
|
ENSP00000352154.5:p.Leu25897=
|
|
ENST00000460472.6:c.77316G>T
(TTN)
|
ENSP00000434586.1:p.Leu25772=
|
|
ENST00000589042.5:c.104511G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34837=
|
|
ENST00000591111.5:c.99588G>T
(TTN)
|
ENSP00000465570.1:p.Leu33196=
|
|
ENST00000615779.4:c.99588G>T
(TTN)
|
ENSP00000483597.1:p.Leu33196=
|
|
NM_001256850.1:c.99588G>T
(TTN)
|
NP_001243779.1:p.Leu33196=
|
|
NM_001267550.2:c.104511G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34837=
|
|
NM_003319.4:c.77316G>T
(TTN)
|
NP_003310.4:p.Leu25772=
|
|
NM_133378.4:c.96807G>T
(TTN)
|
NP_596869.4:p.Leu32269=
|
|
NM_133432.3:c.77691G>T
(TTN)
|
NP_597676.3:p.Leu25897=
|
|
NM_133437.4:c.77892G>T
(TTN)
|
NP_597681.4:p.Leu25964=
|
|
NR_038271.1:n.446+8468C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3628C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103608G>T
(TTN)
|
XP_011510031.1:p.Leu34536=
|
|
XM_011511730.1:c.77502G>T
(TTN)
|
XP_011510032.1:p.Leu25834=
|
|
XM_011511731.1:c.77361G>T
(TTN)
|
XP_011510033.1:p.Leu25787=
|
|
XM_017004819.1:c.103404G>T
(TTN)
|
XP_016860308.1:p.Leu34468=
|
|
XM_017004820.1:c.98802G>T
(TTN)
|
XP_016860309.1:p.Leu32934=
|
|
XM_017004821.1:c.98799G>T
(TTN)
|
XP_016860310.1:p.Leu32933=
|
|
XM_017004822.1:c.95841G>T
(TTN)
|
XP_016860311.1:p.Leu31947=
|
|
XM_017004823.1:c.77457G>T
(TTN)
|
XP_016860312.1:p.Leu25819=
|
|
XM_024453094.1:c.98952G>T
(TTN)
|
XP_024308862.1:p.Leu32984=
|
|
XM_024453095.1:c.98949G>T
(TTN)
|
XP_024308863.1:p.Leu32983=
|
|
XM_024453096.1:c.98382G>T
(TTN)
|
XP_024308864.1:p.Leu32794=
|
|
XM_024453097.1:c.95724G>T
(TTN)
|
XP_024308865.1:p.Leu31908=
|
|
XM_024453098.1:c.95643G>T
(TTN)
|
XP_024308866.1:p.Leu31881=
|
|
XM_024453099.1:c.77406G>T
(TTN)
|
XP_024308867.1:p.Leu25802=
|
|
XM_024453100.1:c.67260G>T
(TTN)
|
XP_024308868.1:p.Leu22420=
|
|