ENST00000342992.11:c.96723G>C
(TTN)
|
ENSP00000343764.6:p.Val32241=
|
|
ENST00000342175.11:c.77808G>C
(TTN)
|
ENSP00000340554.6:p.Val25936=
|
|
ENST00000359218.10:c.77607G>C
(TTN)
|
ENSP00000352154.5:p.Val25869=
|
|
ENST00000342175.10:c.77808G>C
(TTN)
|
ENSP00000340554.6:p.Val25936=
|
|
ENST00000342992.10:c.96723G>C
(TTN)
|
ENSP00000343764.6:p.Val32241=
|
|
ENST00000359218.9:c.77607G>C
(TTN)
|
ENSP00000352154.5:p.Val25869=
|
|
ENST00000460472.6:c.77232G>C
(TTN)
|
ENSP00000434586.1:p.Val25744=
|
|
ENST00000589042.5:c.104427G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val34809=
|
|
ENST00000591111.5:c.99504G>C
(TTN)
|
ENSP00000465570.1:p.Val33168=
|
|
ENST00000615779.4:c.99504G>C
(TTN)
|
ENSP00000483597.1:p.Val33168=
|
|
NM_001256850.1:c.99504G>C
(TTN)
|
NP_001243779.1:p.Val33168=
|
|
NM_001267550.2:c.104427G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val34809=
|
|
NM_003319.4:c.77232G>C
(TTN)
|
NP_003310.4:p.Val25744=
|
|
NM_133378.4:c.96723G>C
(TTN)
|
NP_596869.4:p.Val32241=
|
|
NM_133432.3:c.77607G>C
(TTN)
|
NP_597676.3:p.Val25869=
|
|
NM_133437.4:c.77808G>C
(TTN)
|
NP_597681.4:p.Val25936=
|
|
NR_038271.1:n.446+8552C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3544C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103524G>C
(TTN)
|
XP_011510031.1:p.Val34508=
|
|
XM_011511730.1:c.77418G>C
(TTN)
|
XP_011510032.1:p.Val25806=
|
|
XM_011511731.1:c.77277G>C
(TTN)
|
XP_011510033.1:p.Val25759=
|
|
XM_017004819.1:c.103320G>C
(TTN)
|
XP_016860308.1:p.Val34440=
|
|
XM_017004820.1:c.98718G>C
(TTN)
|
XP_016860309.1:p.Val32906=
|
|
XM_017004821.1:c.98715G>C
(TTN)
|
XP_016860310.1:p.Val32905=
|
|
XM_017004822.1:c.95757G>C
(TTN)
|
XP_016860311.1:p.Val31919=
|
|
XM_017004823.1:c.77373G>C
(TTN)
|
XP_016860312.1:p.Val25791=
|
|
XM_024453094.1:c.98868G>C
(TTN)
|
XP_024308862.1:p.Val32956=
|
|
XM_024453095.1:c.98865G>C
(TTN)
|
XP_024308863.1:p.Val32955=
|
|
XM_024453096.1:c.98298G>C
(TTN)
|
XP_024308864.1:p.Val32766=
|
|
XM_024453097.1:c.95640G>C
(TTN)
|
XP_024308865.1:p.Val31880=
|
|
XM_024453098.1:c.95559G>C
(TTN)
|
XP_024308866.1:p.Val31853=
|
|
XM_024453099.1:c.77322G>C
(TTN)
|
XP_024308867.1:p.Val25774=
|
|
XM_024453100.1:c.67176G>C
(TTN)
|
XP_024308868.1:p.Val22392=
|
|