ENST00000700555.2:n.537G=
|
|
|
ENST00000700557.2:n.126G=
|
|
|
ENST00000700559.2:c.2034G=
|
ENSP00000515065.2:p.Gln678=
|
|
ENST00000546498.2:n.721G=
|
|
|
ENST00000549461.2:n.573G=
|
|
|
ENST00000700555.1:c.465G=
|
ENSP00000515062.1:p.Gln155=
|
|
ENST00000700556.1:c.505G=
|
|
|
ENST00000700557.1:c.45G=
|
ENSP00000515064.1:p.Gln15=
|
|
ENST00000700558.1:n.248G=
|
|
|
ENST00000700559.1:c.1249G=
|
|
|
ENST00000700560.1:n.1249G=
|
|
|
ENST00000700561.1:n.1375G=
|
|
|
ENST00000070846.11:c.2166G=
|
ENSP00000070846.6:p.Gln722=
|
|
ENST00000340811.9:c.2034G=
MANE Select
|
ENSP00000342800.5:p.Gln678=
|
|
ENST00000070846.10:c.2166G=
|
ENSP00000070846.6:p.Gln722=
|
|
ENST00000340811.8:c.2034G=
|
ENSP00000342800.4:p.Gln678=
|
|
ENST00000549461.1:n.480G=
|
|
|
ENST00000613243.1:c.2166G=
|
ENSP00000478295.1:p.Gln722=
|
|
NM_001005242.2:c.2034G=
|
NP_001005242.2:p.Gln678=
|
|
NM_004572.3:c.2166G= , LRG_398t1:c.2166G=
|
NP_004563.2:p.Gln722=
|
|
NM_001005242.3:c.2034G=
MANE Select
|
NP_001005242.2:p.Gln678=
|
|
NM_004572.4:c.2166G=
|
NP_004563.2:p.Gln722=
|
|