ENST00000589419.2:n.978C>A
|
|
|
ENST00000650467.2:c.753C>A
|
ENSP00000496897.2:p.Pro251=
|
|
ENST00000695903.1:c.1088C>A
|
ENSP00000512255.1:p.Pro363Gln
|
|
ENST00000695904.1:c.1088C>A
|
ENSP00000512259.1:p.Pro363Gln
|
|
ENST00000439986.9:c.975C>A
MANE Select
|
ENSP00000404464.2:p.Pro325=
|
|
ENST00000589116.2:n.683C>A
|
|
|
ENST00000649564.1:c.975C>A
|
ENSP00000497183.1:p.Pro325=
|
|
ENST00000650467.1:c.631C>A
|
|
|
ENST00000398179.3:c.765C>A
|
ENSP00000381241.3:p.Pro255=
|
|
ENST00000439986.8:c.975C>A
|
ENSP00000404464.2:p.Pro325=
|
|
ENST00000589116.1:n.683C>A
|
|
|
NM_133459.3:c.975C>A
|
NP_597716.1:p.Pro325=
|
|
XM_005266648.2:c.975C>A
|
XP_005266705.1:p.Pro325=
|
|
NM_133459.4:c.975C>A
MANE Select
|
NP_597716.1:p.Pro325=
|
|
XM_017025556.1:c.1088C>A
|
XP_016881045.1:p.Pro363Gln
|
|
XM_017025557.1:c.1088C>A
|
XP_016881046.1:p.Pro363Gln
|
|
XM_017025558.1:c.975C>A
|
XP_016881047.1:p.Pro325=
|
|
XM_024451091.1:c.975C>A
|
XP_024306859.1:p.Pro325=
|
|
XR_001753142.1:n.1927C>A
|
|
|