ENST00000682520.1:c.877T>C
|
ENSP00000507547.1:n.877T>C
|
|
ENST00000375326.9:c.717T>C
MANE Select
|
ENSP00000364475.5:p.Ala239=
|
|
ENST00000648117.1:c.522T>C
|
ENSP00000498145.1:p.Ala174=
|
|
ENST00000375326.8:c.717T>C
|
ENSP00000364475.4:p.Ala239=
|
|
ENST00000415431.5:c.717T>C
|
ENSP00000408025.1:p.Ala239=
|
|
NM_000507.3:c.717T>C
|
NP_000498.2:p.Ala239=
|
|
NM_001127628.1:c.717T>C
|
NP_001121100.1:p.Ala239=
|
|
XM_006717005.2:c.471T>C
|
XP_006717068.1:p.Ala157=
|
|
XM_006717005.4:c.471T>C
|
XP_006717068.1:p.Ala157=
|
|
NM_000507.4:c.717T>C
MANE Select
|
NP_000498.2:p.Ala239=
|
|
NM_001127628.2:c.717T>C
|
NP_001121100.1:p.Ala239=
|
|