ENST00000342992.11:c.98278G>C
(TTN)
|
ENSP00000343764.6:p.Glu32760Gln
|
|
ENST00000342175.11:c.79363G>C
(TTN)
|
ENSP00000340554.6:p.Glu26455Gln
|
|
ENST00000359218.10:c.79162G>C
(TTN)
|
ENSP00000352154.5:p.Glu26388Gln
|
|
ENST00000342175.10:c.79363G>C
(TTN)
|
ENSP00000340554.6:p.Glu26455Gln
|
|
ENST00000342992.10:c.98278G>C
(TTN)
|
ENSP00000343764.6:p.Glu32760Gln
|
|
ENST00000359218.9:c.79162G>C
(TTN)
|
ENSP00000352154.5:p.Glu26388Gln
|
|
ENST00000460472.6:c.78787G>C
(TTN)
|
ENSP00000434586.1:p.Glu26263Gln
|
|
ENST00000589042.5:c.105982G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35328Gln
|
|
ENST00000591111.5:c.101059G>C
(TTN)
|
ENSP00000465570.1:p.Glu33687Gln
|
|
ENST00000615779.4:c.101059G>C
(TTN)
|
ENSP00000483597.1:p.Glu33687Gln
|
|
NM_001256850.1:c.101059G>C
(TTN)
|
NP_001243779.1:p.Glu33687Gln
|
|
NM_001267550.2:c.105982G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35328Gln
|
|
NM_003319.4:c.78787G>C
(TTN)
|
NP_003310.4:p.Glu26263Gln
|
|
NM_133378.4:c.98278G>C
(TTN)
|
NP_596869.4:p.Glu32760Gln
|
|
NM_133432.3:c.79162G>C
(TTN)
|
NP_597676.3:p.Glu26388Gln
|
|
NM_133437.4:c.79363G>C
(TTN)
|
NP_597681.4:p.Glu26455Gln
|
|
NR_038271.1:n.446+6997C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5099C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105079G>C
(TTN)
|
XP_011510031.1:p.Glu35027Gln
|
|
XM_011511730.1:c.78973G>C
(TTN)
|
XP_011510032.1:p.Glu26325Gln
|
|
XM_011511731.1:c.78832G>C
(TTN)
|
XP_011510033.1:p.Glu26278Gln
|
|
XM_017004819.1:c.104875G>C
(TTN)
|
XP_016860308.1:p.Glu34959Gln
|
|
XM_017004820.1:c.100273G>C
(TTN)
|
XP_016860309.1:p.Glu33425Gln
|
|
XM_017004821.1:c.100270G>C
(TTN)
|
XP_016860310.1:p.Glu33424Gln
|
|
XM_017004822.1:c.97312G>C
(TTN)
|
XP_016860311.1:p.Glu32438Gln
|
|
XM_017004823.1:c.78928G>C
(TTN)
|
XP_016860312.1:p.Glu26310Gln
|
|
XM_024453094.1:c.100423G>C
(TTN)
|
XP_024308862.1:p.Glu33475Gln
|
|
XM_024453095.1:c.100420G>C
(TTN)
|
XP_024308863.1:p.Glu33474Gln
|
|
XM_024453096.1:c.99853G>C
(TTN)
|
XP_024308864.1:p.Glu33285Gln
|
|
XM_024453097.1:c.97195G>C
(TTN)
|
XP_024308865.1:p.Glu32399Gln
|
|
XM_024453098.1:c.97114G>C
(TTN)
|
XP_024308866.1:p.Glu32372Gln
|
|
XM_024453099.1:c.78877G>C
(TTN)
|
XP_024308867.1:p.Glu26293Gln
|
|
XM_024453100.1:c.68731G>C
(TTN)
|
XP_024308868.1:p.Glu22911Gln
|
|