ENST00000359595.8:c.400C>T
MANE Select
|
ENSP00000352606.4:p.Gln134Ter
|
|
ENST00000359595.7:c.400C>T
|
ENSP00000352606.3:p.Gln134Ter
|
|
ENST00000558770.5:c.400C>T
|
ENSP00000456458.1:p.Gln134Ter
|
|
ENST00000562281.1:c.400C>T
|
ENSP00000456985.1:p.Gln134Ter
|
|
ENST00000562889.5:c.586C>T
|
ENSP00000457180.1:p.Gln196Ter
|
|
ENST00000563808.1:n.502C>T
|
|
|
NM_001307952.1:c.586C>T
|
NP_001294881.1:p.Gln196Ter
|
|
NM_178232.2:c.400C>T
|
NP_839946.1:p.Gln134Ter
|
|
NM_178232.3:c.400C>T
|
NP_839946.1:p.Gln134Ter
|
|
XM_011521261.1:c.532C>T
|
XP_011519563.1:p.Gln178Ter
|
|
XR_243204.1:n.615C>T
|
|
|
XR_931756.1:n.721C>T
|
|
|
XM_017021934.2:c.586C>T
|
XP_016877423.1:p.Gln196Ter
|
|
XM_017021935.2:c.21C>T
|
XP_016877424.1:p.Ser7=
|
|
XM_017021936.2:c.21C>T
|
XP_016877425.1:p.Ser7=
|
|
XR_001751098.2:n.733C>T
|
|
|
XR_931756.3:n.734C>T
|
|
|
NM_001307952.2:c.586C>T
|
NP_001294881.1:p.Gln196Ter
|
|
NM_178232.4:c.400C>T
MANE Select
|
NP_839946.1:p.Gln134Ter
|
|