ENST00000367408.6:n.2406A=
|
|
|
ENST00000367409.9:c.9119A=
MANE Select
|
ENSP00000356379.4:p.Tyr3040=
|
|
ENST00000680265.1:c.9341A=
|
ENSP00000505384.1:p.Tyr3114=
|
|
ENST00000680710.1:c.9119A=
|
ENSP00000506676.1:p.Tyr3040=
|
|
ENST00000294732.11:c.4364A=
|
ENSP00000294732.7:p.Tyr1455=
|
|
ENST00000367408.5:c.2114A=
|
ENSP00000356378.1:p.Tyr705=
|
|
ENST00000367409.8:c.9119A=
|
ENSP00000356379.4:p.Tyr3040=
|
|
ENST00000612785.1:c.3077A=
|
ENSP00000479244.1:p.Tyr1026=
|
|
NM_001206846.1:c.4364A=
|
NP_001193775.1:p.Tyr1455=
|
|
NM_018136.4:c.9119A=
|
NP_060606.3:p.Tyr3040=
|
|
NM_018136.5:c.9119A=
MANE Select
|
NP_060606.3:p.Tyr3040=
|
|
NM_001206846.2:c.4364A=
|
NP_001193775.1:p.Tyr1455=
|
|