ENST00000342992.11:c.100150G>A
(TTN)
|
ENSP00000343764.6:p.Asp33384Asn
|
|
ENST00000342175.11:c.81235G>A
(TTN)
|
ENSP00000340554.6:p.Asp27079Asn
|
|
ENST00000359218.10:c.81034G>A
(TTN)
|
ENSP00000352154.5:p.Asp27012Asn
|
|
ENST00000342175.10:c.81235G>A
(TTN)
|
ENSP00000340554.6:p.Asp27079Asn
|
|
ENST00000342992.10:c.100150G>A
(TTN)
|
ENSP00000343764.6:p.Asp33384Asn
|
|
ENST00000359218.9:c.81034G>A
(TTN)
|
ENSP00000352154.5:p.Asp27012Asn
|
|
ENST00000460472.6:c.80659G>A
(TTN)
|
ENSP00000434586.1:p.Asp26887Asn
|
|
ENST00000589042.5:c.107854G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35952Asn
|
|
ENST00000591111.5:c.102931G>A
(TTN)
|
ENSP00000465570.1:p.Asp34311Asn
|
|
ENST00000615779.4:c.102931G>A
(TTN)
|
ENSP00000483597.1:p.Asp34311Asn
|
|
NM_001256850.1:c.102931G>A
(TTN)
|
NP_001243779.1:p.Asp34311Asn
|
|
NM_001267550.2:c.107854G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35952Asn
|
|
NM_003319.4:c.80659G>A
(TTN)
|
NP_003310.4:p.Asp26887Asn
|
|
NM_133378.4:c.100150G>A
(TTN)
|
NP_596869.4:p.Asp33384Asn
|
|
NM_133432.3:c.81034G>A
(TTN)
|
NP_597676.3:p.Asp27012Asn
|
|
NM_133437.4:c.81235G>A
(TTN)
|
NP_597681.4:p.Asp27079Asn
|
|
NR_038271.1:n.446+3498C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3498C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.106951G>A
(TTN)
|
XP_011510031.1:p.Asp35651Asn
|
|
XM_011511730.1:c.80845G>A
(TTN)
|
XP_011510032.1:p.Asp26949Asn
|
|
XM_011511731.1:c.80704G>A
(TTN)
|
XP_011510033.1:p.Asp26902Asn
|
|
XM_017004819.1:c.106747G>A
(TTN)
|
XP_016860308.1:p.Asp35583Asn
|
|
XM_017004820.1:c.102145G>A
(TTN)
|
XP_016860309.1:p.Asp34049Asn
|
|
XM_017004821.1:c.102142G>A
(TTN)
|
XP_016860310.1:p.Asp34048Asn
|
|
XM_017004822.1:c.99184G>A
(TTN)
|
XP_016860311.1:p.Asp33062Asn
|
|
XM_017004823.1:c.80800G>A
(TTN)
|
XP_016860312.1:p.Asp26934Asn
|
|
XM_024453094.1:c.102295G>A
(TTN)
|
XP_024308862.1:p.Asp34099Asn
|
|
XM_024453095.1:c.102292G>A
(TTN)
|
XP_024308863.1:p.Asp34098Asn
|
|
XM_024453096.1:c.101725G>A
(TTN)
|
XP_024308864.1:p.Asp33909Asn
|
|
XM_024453097.1:c.99067G>A
(TTN)
|
XP_024308865.1:p.Asp33023Asn
|
|
XM_024453098.1:c.98986G>A
(TTN)
|
XP_024308866.1:p.Asp32996Asn
|
|
XM_024453099.1:c.80749G>A
(TTN)
|
XP_024308867.1:p.Asp26917Asn
|
|
XM_024453100.1:c.70603G>A
(TTN)
|
XP_024308868.1:p.Asp23535Asn
|
|