ENST00000342992.11:c.63635C>A
(TTN)
|
ENSP00000343764.6:p.Thr21212Asn
|
|
ENST00000342175.11:c.44720C>A
(TTN)
|
ENSP00000340554.6:p.Thr14907Asn
|
|
ENST00000359218.10:c.44519C>A
(TTN)
|
ENSP00000352154.5:p.Thr14840Asn
|
|
ENST00000342175.10:c.44720C>A
(TTN)
|
ENSP00000340554.6:p.Thr14907Asn
|
|
ENST00000342992.10:c.63635C>A
(TTN)
|
ENSP00000343764.6:p.Thr21212Asn
|
|
ENST00000359218.9:c.44519C>A
(TTN)
|
ENSP00000352154.5:p.Thr14840Asn
|
|
ENST00000460472.6:c.44144C>A
(TTN)
|
ENSP00000434586.1:p.Thr14715Asn
|
|
ENST00000589042.5:c.71339C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr23780Asn
|
|
ENST00000591111.5:c.66416C>A
(TTN)
|
ENSP00000465570.1:p.Thr22139Asn
|
|
ENST00000615779.4:c.66416C>A
(TTN)
|
ENSP00000483597.1:p.Thr22139Asn
|
|
NM_001256850.1:c.66416C>A
(TTN)
|
NP_001243779.1:p.Thr22139Asn
|
|
NM_001267550.2:c.71339C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr23780Asn
|
|
NM_003319.4:c.44144C>A
(TTN)
|
NP_003310.4:p.Thr14715Asn
|
|
NM_133378.4:c.63635C>A
(TTN)
|
NP_596869.4:p.Thr21212Asn
|
|
NM_133432.3:c.44519C>A
(TTN)
|
NP_597676.3:p.Thr14840Asn
|
|
NM_133437.4:c.44720C>A
(TTN)
|
NP_597681.4:p.Thr14907Asn
|
|
NR_038271.1:n.596+3344G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7779G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.70436C>A
(TTN)
|
XP_011510031.1:p.Thr23479Asn
|
|
XM_011511730.1:c.44330C>A
(TTN)
|
XP_011510032.1:p.Thr14777Asn
|
|
XM_011511731.1:c.44189C>A
(TTN)
|
XP_011510033.1:p.Thr14730Asn
|
|
XM_017004819.1:c.70232C>A
(TTN)
|
XP_016860308.1:p.Thr23411Asn
|
|
XM_017004820.1:c.65630C>A
(TTN)
|
XP_016860309.1:p.Thr21877Asn
|
|
XM_017004821.1:c.65627C>A
(TTN)
|
XP_016860310.1:p.Thr21876Asn
|
|
XM_017004822.1:c.62669C>A
(TTN)
|
XP_016860311.1:p.Thr20890Asn
|
|
XM_017004823.1:c.44285C>A
(TTN)
|
XP_016860312.1:p.Thr14762Asn
|
|
XM_024453094.1:c.65780C>A
(TTN)
|
XP_024308862.1:p.Thr21927Asn
|
|
XM_024453095.1:c.65777C>A
(TTN)
|
XP_024308863.1:p.Thr21926Asn
|
|
XM_024453096.1:c.65210C>A
(TTN)
|
XP_024308864.1:p.Thr21737Asn
|
|
XM_024453097.1:c.62552C>A
(TTN)
|
XP_024308865.1:p.Thr20851Asn
|
|
XM_024453098.1:c.62471C>A
(TTN)
|
XP_024308866.1:p.Thr20824Asn
|
|
XM_024453099.1:c.44234C>A
(TTN)
|
XP_024308867.1:p.Thr14745Asn
|
|
XM_024453100.1:c.34088C>A
(TTN)
|
XP_024308868.1:p.Thr11363Asn
|
|