ENST00000342992.11:c.98432T>C
(TTN)
|
ENSP00000343764.6:p.Phe32811Ser
|
|
ENST00000342175.11:c.79517T>C
(TTN)
|
ENSP00000340554.6:p.Phe26506Ser
|
|
ENST00000359218.10:c.79316T>C
(TTN)
|
ENSP00000352154.5:p.Phe26439Ser
|
|
ENST00000342175.10:c.79517T>C
(TTN)
|
ENSP00000340554.6:p.Phe26506Ser
|
|
ENST00000342992.10:c.98432T>C
(TTN)
|
ENSP00000343764.6:p.Phe32811Ser
|
|
ENST00000359218.9:c.79316T>C
(TTN)
|
ENSP00000352154.5:p.Phe26439Ser
|
|
ENST00000460472.6:c.78941T>C
(TTN)
|
ENSP00000434586.1:p.Phe26314Ser
|
|
ENST00000589042.5:c.106136T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35379Ser
|
|
ENST00000591111.5:c.101213T>C
(TTN)
|
ENSP00000465570.1:p.Phe33738Ser
|
|
ENST00000615779.4:c.101213T>C
(TTN)
|
ENSP00000483597.1:p.Phe33738Ser
|
|
NM_001256850.1:c.101213T>C
(TTN)
|
NP_001243779.1:p.Phe33738Ser
|
|
NM_001267550.2:c.106136T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35379Ser
|
|
NM_003319.4:c.78941T>C
(TTN)
|
NP_003310.4:p.Phe26314Ser
|
|
NM_133378.4:c.98432T>C
(TTN)
|
NP_596869.4:p.Phe32811Ser
|
|
NM_133432.3:c.79316T>C
(TTN)
|
NP_597676.3:p.Phe26439Ser
|
|
NM_133437.4:c.79517T>C
(TTN)
|
NP_597681.4:p.Phe26506Ser
|
|
NR_038271.1:n.446+6843A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5253A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105233T>C
(TTN)
|
XP_011510031.1:p.Phe35078Ser
|
|
XM_011511730.1:c.79127T>C
(TTN)
|
XP_011510032.1:p.Phe26376Ser
|
|
XM_011511731.1:c.78986T>C
(TTN)
|
XP_011510033.1:p.Phe26329Ser
|
|
XM_017004819.1:c.105029T>C
(TTN)
|
XP_016860308.1:p.Phe35010Ser
|
|
XM_017004820.1:c.100427T>C
(TTN)
|
XP_016860309.1:p.Phe33476Ser
|
|
XM_017004821.1:c.100424T>C
(TTN)
|
XP_016860310.1:p.Phe33475Ser
|
|
XM_017004822.1:c.97466T>C
(TTN)
|
XP_016860311.1:p.Phe32489Ser
|
|
XM_017004823.1:c.79082T>C
(TTN)
|
XP_016860312.1:p.Phe26361Ser
|
|
XM_024453094.1:c.100577T>C
(TTN)
|
XP_024308862.1:p.Phe33526Ser
|
|
XM_024453095.1:c.100574T>C
(TTN)
|
XP_024308863.1:p.Phe33525Ser
|
|
XM_024453096.1:c.100007T>C
(TTN)
|
XP_024308864.1:p.Phe33336Ser
|
|
XM_024453097.1:c.97349T>C
(TTN)
|
XP_024308865.1:p.Phe32450Ser
|
|
XM_024453098.1:c.97268T>C
(TTN)
|
XP_024308866.1:p.Phe32423Ser
|
|
XM_024453099.1:c.79031T>C
(TTN)
|
XP_024308867.1:p.Phe26344Ser
|
|
XM_024453100.1:c.68885T>C
(TTN)
|
XP_024308868.1:p.Phe22962Ser
|
|