ENST00000342992.11:c.98354A>G
(TTN)
|
ENSP00000343764.6:p.Asp32785Gly
|
|
ENST00000342175.11:c.79439A>G
(TTN)
|
ENSP00000340554.6:p.Asp26480Gly
|
|
ENST00000359218.10:c.79238A>G
(TTN)
|
ENSP00000352154.5:p.Asp26413Gly
|
|
ENST00000342175.10:c.79439A>G
(TTN)
|
ENSP00000340554.6:p.Asp26480Gly
|
|
ENST00000342992.10:c.98354A>G
(TTN)
|
ENSP00000343764.6:p.Asp32785Gly
|
|
ENST00000359218.9:c.79238A>G
(TTN)
|
ENSP00000352154.5:p.Asp26413Gly
|
|
ENST00000460472.6:c.78863A>G
(TTN)
|
ENSP00000434586.1:p.Asp26288Gly
|
|
ENST00000589042.5:c.106058A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35353Gly
|
|
ENST00000591111.5:c.101135A>G
(TTN)
|
ENSP00000465570.1:p.Asp33712Gly
|
|
ENST00000615779.4:c.101135A>G
(TTN)
|
ENSP00000483597.1:p.Asp33712Gly
|
|
NM_001256850.1:c.101135A>G
(TTN)
|
NP_001243779.1:p.Asp33712Gly
|
|
NM_001267550.2:c.106058A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35353Gly
|
|
NM_003319.4:c.78863A>G
(TTN)
|
NP_003310.4:p.Asp26288Gly
|
|
NM_133378.4:c.98354A>G
(TTN)
|
NP_596869.4:p.Asp32785Gly
|
|
NM_133432.3:c.79238A>G
(TTN)
|
NP_597676.3:p.Asp26413Gly
|
|
NM_133437.4:c.79439A>G
(TTN)
|
NP_597681.4:p.Asp26480Gly
|
|
NR_038271.1:n.446+6921T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5175T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105155A>G
(TTN)
|
XP_011510031.1:p.Asp35052Gly
|
|
XM_011511730.1:c.79049A>G
(TTN)
|
XP_011510032.1:p.Asp26350Gly
|
|
XM_011511731.1:c.78908A>G
(TTN)
|
XP_011510033.1:p.Asp26303Gly
|
|
XM_017004819.1:c.104951A>G
(TTN)
|
XP_016860308.1:p.Asp34984Gly
|
|
XM_017004820.1:c.100349A>G
(TTN)
|
XP_016860309.1:p.Asp33450Gly
|
|
XM_017004821.1:c.100346A>G
(TTN)
|
XP_016860310.1:p.Asp33449Gly
|
|
XM_017004822.1:c.97388A>G
(TTN)
|
XP_016860311.1:p.Asp32463Gly
|
|
XM_017004823.1:c.79004A>G
(TTN)
|
XP_016860312.1:p.Asp26335Gly
|
|
XM_024453094.1:c.100499A>G
(TTN)
|
XP_024308862.1:p.Asp33500Gly
|
|
XM_024453095.1:c.100496A>G
(TTN)
|
XP_024308863.1:p.Asp33499Gly
|
|
XM_024453096.1:c.99929A>G
(TTN)
|
XP_024308864.1:p.Asp33310Gly
|
|
XM_024453097.1:c.97271A>G
(TTN)
|
XP_024308865.1:p.Asp32424Gly
|
|
XM_024453098.1:c.97190A>G
(TTN)
|
XP_024308866.1:p.Asp32397Gly
|
|
XM_024453099.1:c.78953A>G
(TTN)
|
XP_024308867.1:p.Asp26318Gly
|
|
XM_024453100.1:c.68807A>G
(TTN)
|
XP_024308868.1:p.Asp22936Gly
|
|