ENST00000367408.6:n.1912+14_1912+15dup
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|
|
ENST00000367409.9:c.3870+14_3870+15dup
MANE Select
|
ENSP00000356379.4:n.3870+14_3870+15dup
|
|
ENST00000680112.1:n.1940_1941dup
|
|
|
ENST00000680265.1:c.3870+14_3870+15dup
|
ENSP00000505384.1:n.3870+14_3870+15dup
|
|
ENST00000680710.1:c.3870+14_3870+15dup
|
ENSP00000506676.1:n.3870+14_3870+15dup
|
|
ENST00000681879.1:c.3884_3885dup
|
ENSP00000505363.1:p.Glu1296MetfsTer5
|
|
ENST00000294732.11:c.3870+14_3870+15dup
|
ENSP00000294732.7:n.3870+14_3870+15dup
|
|
ENST00000367408.5:c.1620+14_1620+15dup
|
ENSP00000356378.1:n.1620+14_1620+15dup
|
|
ENST00000367409.8:c.3870+14_3870+15dup
|
ENSP00000356379.4:n.3870+14_3870+15dup
|
|
ENST00000612785.1:c.562-19254_562-19253dup
|
ENSP00000479244.1:n.562-19254_562-19253dup
|
|
NM_001206846.1:c.3870+14_3870+15dup
|
NP_001193775.1:n.3870+14_3870+15dup
|
|
NM_018136.4:c.3870+14_3870+15dup
|
NP_060606.3:n.3870+14_3870+15dup
|
|
NM_018136.5:c.3870+14_3870+15dup
MANE Select
|
NP_060606.3:n.3870+14_3870+15dup
|
|
NM_001206846.2:c.3870+14_3870+15dup
|
NP_001193775.1:n.3870+14_3870+15dup
|
|