ENST00000367408.6:n.2108-8094T=
|
|
|
ENST00000367409.9:c.4993T=
MANE Select
|
ENSP00000356379.4:p.Tyr1665=
|
|
ENST00000680265.1:c.4993T=
|
ENSP00000505384.1:p.Tyr1665=
|
|
ENST00000680710.1:c.4993T=
|
ENSP00000506676.1:p.Tyr1665=
|
|
ENST00000294732.11:c.4066-8094T=
|
ENSP00000294732.7:n.4066-8094T=
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|
ENST00000367408.5:c.1816-8094T=
|
ENSP00000356378.1:n.1816-8094T=
|
|
ENST00000367409.8:c.4993T=
|
ENSP00000356379.4:p.Tyr1665=
|
|
ENST00000612785.1:c.562-1611T=
|
ENSP00000479244.1:n.562-1611T=
|
|
NM_001206846.1:c.4066-8094T=
|
NP_001193775.1:n.4066-8094T=
|
|
NM_018136.4:c.4993T=
|
NP_060606.3:p.Tyr1665=
|
|
NM_018136.5:c.4993T=
MANE Select
|
NP_060606.3:p.Tyr1665=
|
|
NM_001206846.2:c.4066-8094T=
|
NP_001193775.1:n.4066-8094T=
|
|