ENST00000342992.11:c.100191T>C
(TTN)
|
ENSP00000343764.6:p.Asp33397=
|
|
ENST00000342175.11:c.81276T>C
(TTN)
|
ENSP00000340554.6:p.Asp27092=
|
|
ENST00000359218.10:c.81075T>C
(TTN)
|
ENSP00000352154.5:p.Asp27025=
|
|
ENST00000342175.10:c.81276T>C
(TTN)
|
ENSP00000340554.6:p.Asp27092=
|
|
ENST00000342992.10:c.100191T>C
(TTN)
|
ENSP00000343764.6:p.Asp33397=
|
|
ENST00000359218.9:c.81075T>C
(TTN)
|
ENSP00000352154.5:p.Asp27025=
|
|
ENST00000460472.6:c.80700T>C
(TTN)
|
ENSP00000434586.1:p.Asp26900=
|
|
ENST00000589042.5:c.107895T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35965=
|
|
ENST00000591111.5:c.102972T>C
(TTN)
|
ENSP00000465570.1:p.Asp34324=
|
|
ENST00000615779.4:c.102972T>C
(TTN)
|
ENSP00000483597.1:p.Asp34324=
|
|
NM_001256850.1:c.102972T>C
(TTN)
|
NP_001243779.1:p.Asp34324=
|
|
NM_001267550.2:c.107895T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35965=
|
|
NM_003319.4:c.80700T>C
(TTN)
|
NP_003310.4:p.Asp26900=
|
|
NM_133378.4:c.100191T>C
(TTN)
|
NP_596869.4:p.Asp33397=
|
|
NM_133432.3:c.81075T>C
(TTN)
|
NP_597676.3:p.Asp27025=
|
|
NM_133437.4:c.81276T>C
(TTN)
|
NP_597681.4:p.Asp27092=
|
|
NR_038271.1:n.446+3457A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3457A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.106992T>C
(TTN)
|
XP_011510031.1:p.Asp35664=
|
|
XM_011511730.1:c.80886T>C
(TTN)
|
XP_011510032.1:p.Asp26962=
|
|
XM_011511731.1:c.80745T>C
(TTN)
|
XP_011510033.1:p.Asp26915=
|
|
XM_017004819.1:c.106788T>C
(TTN)
|
XP_016860308.1:p.Asp35596=
|
|
XM_017004820.1:c.102186T>C
(TTN)
|
XP_016860309.1:p.Asp34062=
|
|
XM_017004821.1:c.102183T>C
(TTN)
|
XP_016860310.1:p.Asp34061=
|
|
XM_017004822.1:c.99225T>C
(TTN)
|
XP_016860311.1:p.Asp33075=
|
|
XM_017004823.1:c.80841T>C
(TTN)
|
XP_016860312.1:p.Asp26947=
|
|
XM_024453094.1:c.102336T>C
(TTN)
|
XP_024308862.1:p.Asp34112=
|
|
XM_024453095.1:c.102333T>C
(TTN)
|
XP_024308863.1:p.Asp34111=
|
|
XM_024453096.1:c.101766T>C
(TTN)
|
XP_024308864.1:p.Asp33922=
|
|
XM_024453097.1:c.99108T>C
(TTN)
|
XP_024308865.1:p.Asp33036=
|
|
XM_024453098.1:c.99027T>C
(TTN)
|
XP_024308866.1:p.Asp33009=
|
|
XM_024453099.1:c.80790T>C
(TTN)
|
XP_024308867.1:p.Asp26930=
|
|
XM_024453100.1:c.70644T>C
(TTN)
|
XP_024308868.1:p.Asp23548=
|
|