ENST00000342992.11:c.41650G>A
(TTN)
|
ENSP00000343764.6:p.Gly13884Ser
|
|
ENST00000342175.11:c.22735G>A
(TTN)
|
ENSP00000340554.6:p.Gly7579Ser
|
|
ENST00000359218.10:c.22534G>A
(TTN)
|
ENSP00000352154.5:p.Gly7512Ser
|
|
ENST00000342175.10:c.22735G>A
(TTN)
|
ENSP00000340554.6:p.Gly7579Ser
|
|
ENST00000342992.10:c.41650G>A
(TTN)
|
ENSP00000343764.6:p.Gly13884Ser
|
|
ENST00000359218.9:c.22534G>A
(TTN)
|
ENSP00000352154.5:p.Gly7512Ser
|
|
ENST00000460472.6:c.22159G>A
(TTN)
|
ENSP00000434586.1:p.Gly7387Ser
|
|
ENST00000589042.5:c.49354G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly16452Ser
|
|
ENST00000591111.5:c.44431G>A
(TTN)
|
ENSP00000465570.1:p.Gly14811Ser
|
|
ENST00000615779.4:c.44431G>A
(TTN)
|
ENSP00000483597.1:p.Gly14811Ser
|
|
NM_001256850.1:c.44431G>A
(TTN)
|
NP_001243779.1:p.Gly14811Ser
|
|
NM_001267550.2:c.49354G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly16452Ser
|
|
NM_003319.4:c.22159G>A
(TTN)
|
NP_003310.4:p.Gly7387Ser
|
|
NM_133378.4:c.41650G>A
(TTN)
|
NP_596869.4:p.Gly13884Ser
|
|
NM_133432.3:c.22534G>A
(TTN)
|
NP_597676.3:p.Gly7512Ser
|
|
NM_133437.4:c.22735G>A
(TTN)
|
NP_597681.4:p.Gly7579Ser
|
|
NR_038271.1:n.783-106C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.48451G>A
(TTN)
|
XP_011510031.1:p.Gly16151Ser
|
|
XM_011511730.1:c.22345G>A
(TTN)
|
XP_011510032.1:p.Gly7449Ser
|
|
XM_011511731.1:c.22204G>A
(TTN)
|
XP_011510033.1:p.Gly7402Ser
|
|
XM_017004819.1:c.48247G>A
(TTN)
|
XP_016860308.1:p.Gly16083Ser
|
|
XM_017004820.1:c.43645G>A
(TTN)
|
XP_016860309.1:p.Gly14549Ser
|
|
XM_017004821.1:c.43642G>A
(TTN)
|
XP_016860310.1:p.Gly14548Ser
|
|
XM_017004822.1:c.40684G>A
(TTN)
|
XP_016860311.1:p.Gly13562Ser
|
|
XM_017004823.1:c.22300G>A
(TTN)
|
XP_016860312.1:p.Gly7434Ser
|
|
XM_024453094.1:c.43795G>A
(TTN)
|
XP_024308862.1:p.Gly14599Ser
|
|
XM_024453095.1:c.43792G>A
(TTN)
|
XP_024308863.1:p.Gly14598Ser
|
|
XM_024453096.1:c.43225G>A
(TTN)
|
XP_024308864.1:p.Gly14409Ser
|
|
XM_024453097.1:c.40567G>A
(TTN)
|
XP_024308865.1:p.Gly13523Ser
|
|
XM_024453098.1:c.40486G>A
(TTN)
|
XP_024308866.1:p.Gly13496Ser
|
|
XM_024453099.1:c.22249G>A
(TTN)
|
XP_024308867.1:p.Gly7417Ser
|
|
XM_024453100.1:c.12103G>A
(TTN)
|
XP_024308868.1:p.Gly4035Ser
|
|