ENST00000342992.11:c.60825T>C
(TTN)
|
ENSP00000343764.6:p.Asp20275=
|
|
ENST00000342175.11:c.41910T>C
(TTN)
|
ENSP00000340554.6:p.Asp13970=
|
|
ENST00000359218.10:c.41709T>C
(TTN)
|
ENSP00000352154.5:p.Asp13903=
|
|
ENST00000342175.10:c.41910T>C
(TTN)
|
ENSP00000340554.6:p.Asp13970=
|
|
ENST00000342992.10:c.60825T>C
(TTN)
|
ENSP00000343764.6:p.Asp20275=
|
|
ENST00000359218.9:c.41709T>C
(TTN)
|
ENSP00000352154.5:p.Asp13903=
|
|
ENST00000460472.6:c.41334T>C
(TTN)
|
ENSP00000434586.1:p.Asp13778=
|
|
ENST00000589042.5:c.68529T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp22843=
|
|
ENST00000591111.5:c.63606T>C
(TTN)
|
ENSP00000465570.1:p.Asp21202=
|
|
ENST00000615779.4:c.63606T>C
(TTN)
|
ENSP00000483597.1:p.Asp21202=
|
|
NM_001256850.1:c.63606T>C
(TTN)
|
NP_001243779.1:p.Asp21202=
|
|
NM_001267550.2:c.68529T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp22843=
|
|
NM_003319.4:c.41334T>C
(TTN)
|
NP_003310.4:p.Asp13778=
|
|
NM_133378.4:c.60825T>C
(TTN)
|
NP_596869.4:p.Asp20275=
|
|
NM_133432.3:c.41709T>C
(TTN)
|
NP_597676.3:p.Asp13903=
|
|
NM_133437.4:c.41910T>C
(TTN)
|
NP_597681.4:p.Asp13970=
|
|
NR_038271.1:n.596+6448A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4675A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.67626T>C
(TTN)
|
XP_011510031.1:p.Asp22542=
|
|
XM_011511730.1:c.41520T>C
(TTN)
|
XP_011510032.1:p.Asp13840=
|
|
XM_011511731.1:c.41379T>C
(TTN)
|
XP_011510033.1:p.Asp13793=
|
|
XM_017004819.1:c.67422T>C
(TTN)
|
XP_016860308.1:p.Asp22474=
|
|
XM_017004820.1:c.62820T>C
(TTN)
|
XP_016860309.1:p.Asp20940=
|
|
XM_017004821.1:c.62817T>C
(TTN)
|
XP_016860310.1:p.Asp20939=
|
|
XM_017004822.1:c.59859T>C
(TTN)
|
XP_016860311.1:p.Asp19953=
|
|
XM_017004823.1:c.41475T>C
(TTN)
|
XP_016860312.1:p.Asp13825=
|
|
XM_024453094.1:c.62970T>C
(TTN)
|
XP_024308862.1:p.Asp20990=
|
|
XM_024453095.1:c.62967T>C
(TTN)
|
XP_024308863.1:p.Asp20989=
|
|
XM_024453096.1:c.62400T>C
(TTN)
|
XP_024308864.1:p.Asp20800=
|
|
XM_024453097.1:c.59742T>C
(TTN)
|
XP_024308865.1:p.Asp19914=
|
|
XM_024453098.1:c.59661T>C
(TTN)
|
XP_024308866.1:p.Asp19887=
|
|
XM_024453099.1:c.41424T>C
(TTN)
|
XP_024308867.1:p.Asp13808=
|
|
XM_024453100.1:c.31278T>C
(TTN)
|
XP_024308868.1:p.Asp10426=
|
|