ENST00000392492.8:c.252G=
MANE Select
|
ENSP00000376282.2:p.Trp84=
|
|
ENST00000250615.7:c.387G=
|
ENSP00000250615.2:p.Trp129=
|
|
ENST00000392492.7:c.252G=
|
ENSP00000376282.2:p.Trp84=
|
|
ENST00000585649.1:c.366G=
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ENSP00000468717.1:p.Trp122=
|
|
ENST00000587798.1:c.*29G=
|
ENSP00000468239.1:n.*29G=
|
|
NM_001088.2:c.252G=
|
NP_001079.1:p.Trp84=
|
|
NM_001166579.1:c.387G=
|
NP_001160051.1:p.Trp129=
|
|
NR_110548.1:n.563G=
|
|
|
XM_011524415.1:c.252G=
|
XP_011522717.1:p.Trp84=
|
|
XM_011524416.1:c.459G=
|
XP_011522718.1:p.Trp153=
|
|
XM_011524417.1:c.459G=
|
XP_011522719.1:p.Trp153=
|
|
XM_011524418.1:c.459G=
|
XP_011522720.1:p.Trp153=
|
|
XM_011524419.1:c.459G=
|
XP_011522721.1:p.Trp153=
|
|
XM_011524420.1:c.459G=
|
XP_011522722.1:p.Trp153=
|
|
XM_011524421.1:c.459G=
|
XP_011522723.1:p.Trp153=
|
|
XM_011524422.1:c.342G=
|
XP_011522724.1:p.Trp114=
|
|
XM_011524423.1:c.252G=
|
XP_011522725.1:p.Trp84=
|
|
XM_017024259.1:c.366G=
|
XP_016879748.1:p.Trp122=
|
|
NM_001088.3:c.252G=
MANE Select
|
NP_001079.1:p.Trp84=
|
|
NR_110548.2:n.508G=
|
|
|
NM_001166579.2:c.387G=
|
NP_001160051.1:p.Trp129=
|
|