ENST00000682520.1:c.980G>T
|
ENSP00000507547.1:n.980G>T
|
|
ENST00000375326.9:c.820G>T
MANE Select
|
ENSP00000364475.5:p.Gly274Ter
|
|
ENST00000648117.1:c.625G>T
|
ENSP00000498145.1:p.Gly209Ter
|
|
ENST00000375326.8:c.820G>T
|
ENSP00000364475.4:p.Gly274Ter
|
|
ENST00000415431.5:c.820G>T
|
ENSP00000408025.1:p.Gly274Ter
|
|
NM_000507.3:c.820G>T
|
NP_000498.2:p.Gly274Ter
|
|
NM_001127628.1:c.820G>T
|
NP_001121100.1:p.Gly274Ter
|
|
XM_006717005.2:c.574G>T
|
XP_006717068.1:p.Gly192Ter
|
|
XM_006717005.4:c.574G>T
|
XP_006717068.1:p.Gly192Ter
|
|
NM_000507.4:c.820G>T
MANE Select
|
NP_000498.2:p.Gly274Ter
|
|
NM_001127628.2:c.820G>T
|
NP_001121100.1:p.Gly274Ter
|
|