ENST00000342992.11:c.98616A>C
(TTN)
|
ENSP00000343764.6:p.Ala32872=
|
|
ENST00000342175.11:c.79701A>C
(TTN)
|
ENSP00000340554.6:p.Ala26567=
|
|
ENST00000359218.10:c.79500A>C
(TTN)
|
ENSP00000352154.5:p.Ala26500=
|
|
ENST00000342175.10:c.79701A>C
(TTN)
|
ENSP00000340554.6:p.Ala26567=
|
|
ENST00000342992.10:c.98616A>C
(TTN)
|
ENSP00000343764.6:p.Ala32872=
|
|
ENST00000359218.9:c.79500A>C
(TTN)
|
ENSP00000352154.5:p.Ala26500=
|
|
ENST00000460472.6:c.79125A>C
(TTN)
|
ENSP00000434586.1:p.Ala26375=
|
|
ENST00000589042.5:c.106320A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35440=
|
|
ENST00000591111.5:c.101397A>C
(TTN)
|
ENSP00000465570.1:p.Ala33799=
|
|
ENST00000615779.4:c.101397A>C
(TTN)
|
ENSP00000483597.1:p.Ala33799=
|
|
NM_001256850.1:c.101397A>C
(TTN)
|
NP_001243779.1:p.Ala33799=
|
|
NM_001267550.2:c.106320A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35440=
|
|
NM_003319.4:c.79125A>C
(TTN)
|
NP_003310.4:p.Ala26375=
|
|
NM_133378.4:c.98616A>C
(TTN)
|
NP_596869.4:p.Ala32872=
|
|
NM_133432.3:c.79500A>C
(TTN)
|
NP_597676.3:p.Ala26500=
|
|
NM_133437.4:c.79701A>C
(TTN)
|
NP_597681.4:p.Ala26567=
|
|
NR_038271.1:n.446+6659T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5437T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105417A>C
(TTN)
|
XP_011510031.1:p.Ala35139=
|
|
XM_011511730.1:c.79311A>C
(TTN)
|
XP_011510032.1:p.Ala26437=
|
|
XM_011511731.1:c.79170A>C
(TTN)
|
XP_011510033.1:p.Ala26390=
|
|
XM_017004819.1:c.105213A>C
(TTN)
|
XP_016860308.1:p.Ala35071=
|
|
XM_017004820.1:c.100611A>C
(TTN)
|
XP_016860309.1:p.Ala33537=
|
|
XM_017004821.1:c.100608A>C
(TTN)
|
XP_016860310.1:p.Ala33536=
|
|
XM_017004822.1:c.97650A>C
(TTN)
|
XP_016860311.1:p.Ala32550=
|
|
XM_017004823.1:c.79266A>C
(TTN)
|
XP_016860312.1:p.Ala26422=
|
|
XM_024453094.1:c.100761A>C
(TTN)
|
XP_024308862.1:p.Ala33587=
|
|
XM_024453095.1:c.100758A>C
(TTN)
|
XP_024308863.1:p.Ala33586=
|
|
XM_024453096.1:c.100191A>C
(TTN)
|
XP_024308864.1:p.Ala33397=
|
|
XM_024453097.1:c.97533A>C
(TTN)
|
XP_024308865.1:p.Ala32511=
|
|
XM_024453098.1:c.97452A>C
(TTN)
|
XP_024308866.1:p.Ala32484=
|
|
XM_024453099.1:c.79215A>C
(TTN)
|
XP_024308867.1:p.Ala26405=
|
|
XM_024453100.1:c.69069A>C
(TTN)
|
XP_024308868.1:p.Ala23023=
|
|