ENST00000342992.11:c.98698C>G
(TTN)
|
ENSP00000343764.6:p.Leu32900Val
|
|
ENST00000342175.11:c.79783C>G
(TTN)
|
ENSP00000340554.6:p.Leu26595Val
|
|
ENST00000359218.10:c.79582C>G
(TTN)
|
ENSP00000352154.5:p.Leu26528Val
|
|
ENST00000342175.10:c.79783C>G
(TTN)
|
ENSP00000340554.6:p.Leu26595Val
|
|
ENST00000342992.10:c.98698C>G
(TTN)
|
ENSP00000343764.6:p.Leu32900Val
|
|
ENST00000359218.9:c.79582C>G
(TTN)
|
ENSP00000352154.5:p.Leu26528Val
|
|
ENST00000460472.6:c.79207C>G
(TTN)
|
ENSP00000434586.1:p.Leu26403Val
|
|
ENST00000589042.5:c.106402C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35468Val
|
|
ENST00000591111.5:c.101479C>G
(TTN)
|
ENSP00000465570.1:p.Leu33827Val
|
|
ENST00000615779.4:c.101479C>G
(TTN)
|
ENSP00000483597.1:p.Leu33827Val
|
|
NM_001256850.1:c.101479C>G
(TTN)
|
NP_001243779.1:p.Leu33827Val
|
|
NM_001267550.2:c.106402C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35468Val
|
|
NM_003319.4:c.79207C>G
(TTN)
|
NP_003310.4:p.Leu26403Val
|
|
NM_133378.4:c.98698C>G
(TTN)
|
NP_596869.4:p.Leu32900Val
|
|
NM_133432.3:c.79582C>G
(TTN)
|
NP_597676.3:p.Leu26528Val
|
|
NM_133437.4:c.79783C>G
(TTN)
|
NP_597681.4:p.Leu26595Val
|
|
NR_038271.1:n.446+6453G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5643G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105499C>G
(TTN)
|
XP_011510031.1:p.Leu35167Val
|
|
XM_011511730.1:c.79393C>G
(TTN)
|
XP_011510032.1:p.Leu26465Val
|
|
XM_011511731.1:c.79252C>G
(TTN)
|
XP_011510033.1:p.Leu26418Val
|
|
XM_017004819.1:c.105295C>G
(TTN)
|
XP_016860308.1:p.Leu35099Val
|
|
XM_017004820.1:c.100693C>G
(TTN)
|
XP_016860309.1:p.Leu33565Val
|
|
XM_017004821.1:c.100690C>G
(TTN)
|
XP_016860310.1:p.Leu33564Val
|
|
XM_017004822.1:c.97732C>G
(TTN)
|
XP_016860311.1:p.Leu32578Val
|
|
XM_017004823.1:c.79348C>G
(TTN)
|
XP_016860312.1:p.Leu26450Val
|
|
XM_024453094.1:c.100843C>G
(TTN)
|
XP_024308862.1:p.Leu33615Val
|
|
XM_024453095.1:c.100840C>G
(TTN)
|
XP_024308863.1:p.Leu33614Val
|
|
XM_024453096.1:c.100273C>G
(TTN)
|
XP_024308864.1:p.Leu33425Val
|
|
XM_024453097.1:c.97615C>G
(TTN)
|
XP_024308865.1:p.Leu32539Val
|
|
XM_024453098.1:c.97534C>G
(TTN)
|
XP_024308866.1:p.Leu32512Val
|
|
XM_024453099.1:c.79297C>G
(TTN)
|
XP_024308867.1:p.Leu26433Val
|
|
XM_024453100.1:c.69151C>G
(TTN)
|
XP_024308868.1:p.Leu23051Val
|
|