ENST00000342992.11:c.64461C>A
(TTN)
|
ENSP00000343764.6:p.Gly21487=
|
|
ENST00000342175.11:c.45546C>A
(TTN)
|
ENSP00000340554.6:p.Gly15182=
|
|
ENST00000359218.10:c.45345C>A
(TTN)
|
ENSP00000352154.5:p.Gly15115=
|
|
ENST00000342175.10:c.45546C>A
(TTN)
|
ENSP00000340554.6:p.Gly15182=
|
|
ENST00000342992.10:c.64461C>A
(TTN)
|
ENSP00000343764.6:p.Gly21487=
|
|
ENST00000359218.9:c.45345C>A
(TTN)
|
ENSP00000352154.5:p.Gly15115=
|
|
ENST00000460472.6:c.44970C>A
(TTN)
|
ENSP00000434586.1:p.Gly14990=
|
|
ENST00000589042.5:c.72165C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly24055=
|
|
ENST00000591111.5:c.67242C>A
(TTN)
|
ENSP00000465570.1:p.Gly22414=
|
|
ENST00000615779.4:c.67242C>A
(TTN)
|
ENSP00000483597.1:p.Gly22414=
|
|
NM_001256850.1:c.67242C>A
(TTN)
|
NP_001243779.1:p.Gly22414=
|
|
NM_001267550.2:c.72165C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly24055=
|
|
NM_003319.4:c.44970C>A
(TTN)
|
NP_003310.4:p.Gly14990=
|
|
NM_133378.4:c.64461C>A
(TTN)
|
NP_596869.4:p.Gly21487=
|
|
NM_133432.3:c.45345C>A
(TTN)
|
NP_597676.3:p.Gly15115=
|
|
NM_133437.4:c.45546C>A
(TTN)
|
NP_597681.4:p.Gly15182=
|
|
NR_038271.1:n.596+2518G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8605G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.71262C>A
(TTN)
|
XP_011510031.1:p.Gly23754=
|
|
XM_011511730.1:c.45156C>A
(TTN)
|
XP_011510032.1:p.Gly15052=
|
|
XM_011511731.1:c.45015C>A
(TTN)
|
XP_011510033.1:p.Gly15005=
|
|
XM_017004819.1:c.71058C>A
(TTN)
|
XP_016860308.1:p.Gly23686=
|
|
XM_017004820.1:c.66456C>A
(TTN)
|
XP_016860309.1:p.Gly22152=
|
|
XM_017004821.1:c.66453C>A
(TTN)
|
XP_016860310.1:p.Gly22151=
|
|
XM_017004822.1:c.63495C>A
(TTN)
|
XP_016860311.1:p.Gly21165=
|
|
XM_017004823.1:c.45111C>A
(TTN)
|
XP_016860312.1:p.Gly15037=
|
|
XM_024453094.1:c.66606C>A
(TTN)
|
XP_024308862.1:p.Gly22202=
|
|
XM_024453095.1:c.66603C>A
(TTN)
|
XP_024308863.1:p.Gly22201=
|
|
XM_024453096.1:c.66036C>A
(TTN)
|
XP_024308864.1:p.Gly22012=
|
|
XM_024453097.1:c.63378C>A
(TTN)
|
XP_024308865.1:p.Gly21126=
|
|
XM_024453098.1:c.63297C>A
(TTN)
|
XP_024308866.1:p.Gly21099=
|
|
XM_024453099.1:c.45060C>A
(TTN)
|
XP_024308867.1:p.Gly15020=
|
|
XM_024453100.1:c.34914C>A
(TTN)
|
XP_024308868.1:p.Gly11638=
|
|