ENST00000342992.11:c.94847A>G
(TTN)
|
ENSP00000343764.6:p.Glu31616Gly
|
|
ENST00000342175.11:c.75932A>G
(TTN)
|
ENSP00000340554.6:p.Glu25311Gly
|
|
ENST00000359218.10:c.75731A>G
(TTN)
|
ENSP00000352154.5:p.Glu25244Gly
|
|
ENST00000342175.10:c.75932A>G
(TTN)
|
ENSP00000340554.6:p.Glu25311Gly
|
|
ENST00000342992.10:c.94847A>G
(TTN)
|
ENSP00000343764.6:p.Glu31616Gly
|
|
ENST00000359218.9:c.75731A>G
(TTN)
|
ENSP00000352154.5:p.Glu25244Gly
|
|
ENST00000460472.6:c.75356A>G
(TTN)
|
ENSP00000434586.1:p.Glu25119Gly
|
|
ENST00000589042.5:c.102551A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34184Gly
|
|
ENST00000591111.5:c.97628A>G
(TTN)
|
ENSP00000465570.1:p.Glu32543Gly
|
|
ENST00000615779.4:c.97628A>G
(TTN)
|
ENSP00000483597.1:p.Glu32543Gly
|
|
NM_001256850.1:c.97628A>G
(TTN)
|
NP_001243779.1:p.Glu32543Gly
|
|
NM_001267550.2:c.102551A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34184Gly
|
|
NM_003319.4:c.75356A>G
(TTN)
|
NP_003310.4:p.Glu25119Gly
|
|
NM_133378.4:c.94847A>G
(TTN)
|
NP_596869.4:p.Glu31616Gly
|
|
NM_133432.3:c.75731A>G
(TTN)
|
NP_597676.3:p.Glu25244Gly
|
|
NM_133437.4:c.75932A>G
(TTN)
|
NP_597681.4:p.Glu25311Gly
|
|
NR_038271.1:n.446+10428T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-1668T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.101648A>G
(TTN)
|
XP_011510031.1:p.Glu33883Gly
|
|
XM_011511730.1:c.75542A>G
(TTN)
|
XP_011510032.1:p.Glu25181Gly
|
|
XM_011511731.1:c.75401A>G
(TTN)
|
XP_011510033.1:p.Glu25134Gly
|
|
XM_017004819.1:c.101444A>G
(TTN)
|
XP_016860308.1:p.Glu33815Gly
|
|
XM_017004820.1:c.96842A>G
(TTN)
|
XP_016860309.1:p.Glu32281Gly
|
|
XM_017004821.1:c.96839A>G
(TTN)
|
XP_016860310.1:p.Glu32280Gly
|
|
XM_017004822.1:c.93881A>G
(TTN)
|
XP_016860311.1:p.Glu31294Gly
|
|
XM_017004823.1:c.75497A>G
(TTN)
|
XP_016860312.1:p.Glu25166Gly
|
|
XM_024453094.1:c.96992A>G
(TTN)
|
XP_024308862.1:p.Glu32331Gly
|
|
XM_024453095.1:c.96989A>G
(TTN)
|
XP_024308863.1:p.Glu32330Gly
|
|
XM_024453096.1:c.96422A>G
(TTN)
|
XP_024308864.1:p.Glu32141Gly
|
|
XM_024453097.1:c.93764A>G
(TTN)
|
XP_024308865.1:p.Glu31255Gly
|
|
XM_024453098.1:c.93683A>G
(TTN)
|
XP_024308866.1:p.Glu31228Gly
|
|
XM_024453099.1:c.75446A>G
(TTN)
|
XP_024308867.1:p.Glu25149Gly
|
|
XM_024453100.1:c.65300A>G
(TTN)
|
XP_024308868.1:p.Glu21767Gly
|
|