ENST00000342992.11:c.39555G>C
(TTN)
|
ENSP00000343764.6:p.Arg13185Ser
|
|
ENST00000342175.11:c.20640G>C
(TTN)
|
ENSP00000340554.6:p.Arg6880Ser
|
|
ENST00000359218.10:c.20439G>C
(TTN)
|
ENSP00000352154.5:p.Arg6813Ser
|
|
ENST00000342175.10:c.20640G>C
(TTN)
|
ENSP00000340554.6:p.Arg6880Ser
|
|
ENST00000342992.10:c.39555G>C
(TTN)
|
ENSP00000343764.6:p.Arg13185Ser
|
|
ENST00000359218.9:c.20439G>C
(TTN)
|
ENSP00000352154.5:p.Arg6813Ser
|
|
ENST00000460472.6:c.20064G>C
(TTN)
|
ENSP00000434586.1:p.Arg6688Ser
|
|
ENST00000589042.5:c.47259G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg15753Ser
|
|
ENST00000591111.5:c.42336G>C
(TTN)
|
ENSP00000465570.1:p.Arg14112Ser
|
|
ENST00000615779.4:c.42336G>C
(TTN)
|
ENSP00000483597.1:p.Arg14112Ser
|
|
NM_001256850.1:c.42336G>C
(TTN)
|
NP_001243779.1:p.Arg14112Ser
|
|
NM_001267550.2:c.47259G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Arg15753Ser
|
|
NM_003319.4:c.20064G>C
(TTN)
|
NP_003310.4:p.Arg6688Ser
|
|
NM_133378.4:c.39555G>C
(TTN)
|
NP_596869.4:p.Arg13185Ser
|
|
NM_133432.3:c.20439G>C
(TTN)
|
NP_597676.3:p.Arg6813Ser
|
|
NM_133437.4:c.20640G>C
(TTN)
|
NP_597681.4:p.Arg6880Ser
|
|
NR_038271.1:n.1605-1554C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.46356G>C
(TTN)
|
XP_011510031.1:p.Arg15452Ser
|
|
XM_011511730.1:c.20250G>C
(TTN)
|
XP_011510032.1:p.Arg6750Ser
|
|
XM_011511731.1:c.20109G>C
(TTN)
|
XP_011510033.1:p.Arg6703Ser
|
|
XM_017004819.1:c.46152G>C
(TTN)
|
XP_016860308.1:p.Arg15384Ser
|
|
XM_017004820.1:c.41550G>C
(TTN)
|
XP_016860309.1:p.Arg13850Ser
|
|
XM_017004821.1:c.41547G>C
(TTN)
|
XP_016860310.1:p.Arg13849Ser
|
|
XM_017004822.1:c.38589G>C
(TTN)
|
XP_016860311.1:p.Arg12863Ser
|
|
XM_017004823.1:c.20205G>C
(TTN)
|
XP_016860312.1:p.Arg6735Ser
|
|
XM_024453094.1:c.41700G>C
(TTN)
|
XP_024308862.1:p.Arg13900Ser
|
|
XM_024453095.1:c.41697G>C
(TTN)
|
XP_024308863.1:p.Arg13899Ser
|
|
XM_024453096.1:c.41130G>C
(TTN)
|
XP_024308864.1:p.Arg13710Ser
|
|
XM_024453097.1:c.38472G>C
(TTN)
|
XP_024308865.1:p.Arg12824Ser
|
|
XM_024453098.1:c.38391G>C
(TTN)
|
XP_024308866.1:p.Arg12797Ser
|
|
XM_024453099.1:c.20154G>C
(TTN)
|
XP_024308867.1:p.Arg6718Ser
|
|
XM_024453100.1:c.10008G>C
(TTN)
|
XP_024308868.1:p.Arg3336Ser
|
|