ENST00000342992.11:c.67973G>C
(TTN)
|
ENSP00000343764.6:p.Trp22658Ser
|
|
ENST00000342175.11:c.49058G>C
(TTN)
|
ENSP00000340554.6:p.Trp16353Ser
|
|
ENST00000359218.10:c.48857G>C
(TTN)
|
ENSP00000352154.5:p.Trp16286Ser
|
|
ENST00000342175.10:c.49058G>C
(TTN)
|
ENSP00000340554.6:p.Trp16353Ser
|
|
ENST00000342992.10:c.67973G>C
(TTN)
|
ENSP00000343764.6:p.Trp22658Ser
|
|
ENST00000359218.9:c.48857G>C
(TTN)
|
ENSP00000352154.5:p.Trp16286Ser
|
|
ENST00000460472.6:c.48482G>C
(TTN)
|
ENSP00000434586.1:p.Trp16161Ser
|
|
ENST00000589042.5:c.75677G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Trp25226Ser
|
|
ENST00000591111.5:c.70754G>C
(TTN)
|
ENSP00000465570.1:p.Trp23585Ser
|
|
ENST00000615779.4:c.70754G>C
(TTN)
|
ENSP00000483597.1:p.Trp23585Ser
|
|
NM_001256850.1:c.70754G>C
(TTN)
|
NP_001243779.1:p.Trp23585Ser
|
|
NM_001267550.2:c.75677G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Trp25226Ser
|
|
NM_003319.4:c.48482G>C
(TTN)
|
NP_003310.4:p.Trp16161Ser
|
|
NM_133378.4:c.67973G>C
(TTN)
|
NP_596869.4:p.Trp22658Ser
|
|
NM_133432.3:c.48857G>C
(TTN)
|
NP_597676.3:p.Trp16286Ser
|
|
NM_133437.4:c.49058G>C
(TTN)
|
NP_597681.4:p.Trp16353Ser
|
|
NR_038271.1:n.447-845C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12117C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.74774G>C
(TTN)
|
XP_011510031.1:p.Trp24925Ser
|
|
XM_011511730.1:c.48668G>C
(TTN)
|
XP_011510032.1:p.Trp16223Ser
|
|
XM_011511731.1:c.48527G>C
(TTN)
|
XP_011510033.1:p.Trp16176Ser
|
|
XM_017004819.1:c.74570G>C
(TTN)
|
XP_016860308.1:p.Trp24857Ser
|
|
XM_017004820.1:c.69968G>C
(TTN)
|
XP_016860309.1:p.Trp23323Ser
|
|
XM_017004821.1:c.69965G>C
(TTN)
|
XP_016860310.1:p.Trp23322Ser
|
|
XM_017004822.1:c.67007G>C
(TTN)
|
XP_016860311.1:p.Trp22336Ser
|
|
XM_017004823.1:c.48623G>C
(TTN)
|
XP_016860312.1:p.Trp16208Ser
|
|
XM_024453094.1:c.70118G>C
(TTN)
|
XP_024308862.1:p.Trp23373Ser
|
|
XM_024453095.1:c.70115G>C
(TTN)
|
XP_024308863.1:p.Trp23372Ser
|
|
XM_024453096.1:c.69548G>C
(TTN)
|
XP_024308864.1:p.Trp23183Ser
|
|
XM_024453097.1:c.66890G>C
(TTN)
|
XP_024308865.1:p.Trp22297Ser
|
|
XM_024453098.1:c.66809G>C
(TTN)
|
XP_024308866.1:p.Trp22270Ser
|
|
XM_024453099.1:c.48572G>C
(TTN)
|
XP_024308867.1:p.Trp16191Ser
|
|
XM_024453100.1:c.38426G>C
(TTN)
|
XP_024308868.1:p.Trp12809Ser
|
|