ENST00000342992.11:c.53112G>T
(TTN)
|
ENSP00000343764.6:p.Pro17704=
|
|
ENST00000342175.11:c.34197G>T
(TTN)
|
ENSP00000340554.6:p.Pro11399=
|
|
ENST00000359218.10:c.33996G>T
(TTN)
|
ENSP00000352154.5:p.Pro11332=
|
|
ENST00000342175.10:c.34197G>T
(TTN)
|
ENSP00000340554.6:p.Pro11399=
|
|
ENST00000342992.10:c.53112G>T
(TTN)
|
ENSP00000343764.6:p.Pro17704=
|
|
ENST00000359218.9:c.33996G>T
(TTN)
|
ENSP00000352154.5:p.Pro11332=
|
|
ENST00000460472.6:c.33621G>T
(TTN)
|
ENSP00000434586.1:p.Pro11207=
|
|
ENST00000589042.5:c.60816G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro20272=
|
|
ENST00000591111.5:c.55893G>T
(TTN)
|
ENSP00000465570.1:p.Pro18631=
|
|
ENST00000615779.4:c.55893G>T
(TTN)
|
ENSP00000483597.1:p.Pro18631=
|
|
NM_001256850.1:c.55893G>T
(TTN)
|
NP_001243779.1:p.Pro18631=
|
|
NM_001267550.2:c.60816G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro20272=
|
|
NM_003319.4:c.33621G>T
(TTN)
|
NP_003310.4:p.Pro11207=
|
|
NM_133378.4:c.53112G>T
(TTN)
|
NP_596869.4:p.Pro17704=
|
|
NM_133432.3:c.33996G>T
(TTN)
|
NP_597676.3:p.Pro11332=
|
|
NM_133437.4:c.34197G>T
(TTN)
|
NP_597681.4:p.Pro11399=
|
|
NR_038271.1:n.597-6687C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-230C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59913G>T
(TTN)
|
XP_011510031.1:p.Pro19971=
|
|
XM_011511730.1:c.33807G>T
(TTN)
|
XP_011510032.1:p.Pro11269=
|
|
XM_011511731.1:c.33666G>T
(TTN)
|
XP_011510033.1:p.Pro11222=
|
|
XM_017004819.1:c.59709G>T
(TTN)
|
XP_016860308.1:p.Pro19903=
|
|
XM_017004820.1:c.55107G>T
(TTN)
|
XP_016860309.1:p.Pro18369=
|
|
XM_017004821.1:c.55104G>T
(TTN)
|
XP_016860310.1:p.Pro18368=
|
|
XM_017004822.1:c.52146G>T
(TTN)
|
XP_016860311.1:p.Pro17382=
|
|
XM_017004823.1:c.33762G>T
(TTN)
|
XP_016860312.1:p.Pro11254=
|
|
XM_024453094.1:c.55257G>T
(TTN)
|
XP_024308862.1:p.Pro18419=
|
|
XM_024453095.1:c.55254G>T
(TTN)
|
XP_024308863.1:p.Pro18418=
|
|
XM_024453096.1:c.54687G>T
(TTN)
|
XP_024308864.1:p.Pro18229=
|
|
XM_024453097.1:c.52029G>T
(TTN)
|
XP_024308865.1:p.Pro17343=
|
|
XM_024453098.1:c.51948G>T
(TTN)
|
XP_024308866.1:p.Pro17316=
|
|
XM_024453099.1:c.33711G>T
(TTN)
|
XP_024308867.1:p.Pro11237=
|
|
XM_024453100.1:c.23565G>T
(TTN)
|
XP_024308868.1:p.Pro7855=
|
|