ENST00000342992.11:c.88205T>C
(TTN)
|
ENSP00000343764.6:p.Phe29402Ser
|
|
ENST00000342175.11:c.69290T>C
(TTN)
|
ENSP00000340554.6:p.Phe23097Ser
|
|
ENST00000359218.10:c.69089T>C
(TTN)
|
ENSP00000352154.5:p.Phe23030Ser
|
|
ENST00000342175.10:c.69290T>C
(TTN)
|
ENSP00000340554.6:p.Phe23097Ser
|
|
ENST00000342992.10:c.88205T>C
(TTN)
|
ENSP00000343764.6:p.Phe29402Ser
|
|
ENST00000359218.9:c.69089T>C
(TTN)
|
ENSP00000352154.5:p.Phe23030Ser
|
|
ENST00000460472.6:c.68714T>C
(TTN)
|
ENSP00000434586.1:p.Phe22905Ser
|
|
ENST00000589042.5:c.95909T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe31970Ser
|
|
ENST00000591111.5:c.90986T>C
(TTN)
|
ENSP00000465570.1:p.Phe30329Ser
|
|
ENST00000615779.4:c.90986T>C
(TTN)
|
ENSP00000483597.1:p.Phe30329Ser
|
|
NM_001256850.1:c.90986T>C
(TTN)
|
NP_001243779.1:p.Phe30329Ser
|
|
NM_001267550.2:c.95909T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Phe31970Ser
|
|
NM_003319.4:c.68714T>C
(TTN)
|
NP_003310.4:p.Phe22905Ser
|
|
NM_133378.4:c.88205T>C
(TTN)
|
NP_596869.4:p.Phe29402Ser
|
|
NM_133432.3:c.69089T>C
(TTN)
|
NP_597676.3:p.Phe23030Ser
|
|
NM_133437.4:c.69290T>C
(TTN)
|
NP_597681.4:p.Phe23097Ser
|
|
NR_038271.1:n.446+20684A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1959A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95006T>C
(TTN)
|
XP_011510031.1:p.Phe31669Ser
|
|
XM_011511730.1:c.68900T>C
(TTN)
|
XP_011510032.1:p.Phe22967Ser
|
|
XM_011511731.1:c.68759T>C
(TTN)
|
XP_011510033.1:p.Phe22920Ser
|
|
XM_017004819.1:c.94802T>C
(TTN)
|
XP_016860308.1:p.Phe31601Ser
|
|
XM_017004820.1:c.90200T>C
(TTN)
|
XP_016860309.1:p.Phe30067Ser
|
|
XM_017004821.1:c.90197T>C
(TTN)
|
XP_016860310.1:p.Phe30066Ser
|
|
XM_017004822.1:c.87239T>C
(TTN)
|
XP_016860311.1:p.Phe29080Ser
|
|
XM_017004823.1:c.68855T>C
(TTN)
|
XP_016860312.1:p.Phe22952Ser
|
|
XM_024453094.1:c.90350T>C
(TTN)
|
XP_024308862.1:p.Phe30117Ser
|
|
XM_024453095.1:c.90347T>C
(TTN)
|
XP_024308863.1:p.Phe30116Ser
|
|
XM_024453096.1:c.89780T>C
(TTN)
|
XP_024308864.1:p.Phe29927Ser
|
|
XM_024453097.1:c.87122T>C
(TTN)
|
XP_024308865.1:p.Phe29041Ser
|
|
XM_024453098.1:c.87041T>C
(TTN)
|
XP_024308866.1:p.Phe29014Ser
|
|
XM_024453099.1:c.68804T>C
(TTN)
|
XP_024308867.1:p.Phe22935Ser
|
|
XM_024453100.1:c.58658T>C
(TTN)
|
XP_024308868.1:p.Phe19553Ser
|
|