ENST00000682520.1:c.976C=
|
ENSP00000507547.1:n.976C=
|
|
ENST00000375326.9:c.816C=
MANE Select
|
ENSP00000364475.5:p.Pro272=
|
|
ENST00000648117.1:c.621C=
|
ENSP00000498145.1:p.Pro207=
|
|
ENST00000375326.8:c.816C=
|
ENSP00000364475.4:p.Pro272=
|
|
ENST00000415431.5:c.816C=
|
ENSP00000408025.1:p.Pro272=
|
|
NM_000507.3:c.816C=
|
NP_000498.2:p.Pro272=
|
|
NM_001127628.1:c.816C=
|
NP_001121100.1:p.Pro272=
|
|
XM_006717005.2:c.570C=
|
XP_006717068.1:p.Pro190=
|
|
XM_006717005.4:c.570C=
|
XP_006717068.1:p.Pro190=
|
|
NM_000507.4:c.816C=
MANE Select
|
NP_000498.2:p.Pro272=
|
|
NM_001127628.2:c.816C=
|
NP_001121100.1:p.Pro272=
|
|