|
NM_016630.7:c.613C>T
MANE Select
|
NP_057714.1:p.Gln205Ter
|
|
ENST00000204566.7:c.613C>T
MANE Select
|
ENSP00000204566.2:p.Gln205Ter
|
|
NM_001127889.4:c.613C>T
|
NP_001121361.1:p.Gln205Ter
|
|
NM_001127889.5:c.613C>T
|
NP_001121361.1:p.Gln205Ter
|
|
NM_001127890.4:c.532C>T
|
NP_001121362.1:p.Gln178Ter
|
|
NM_001127890.5:c.532C>T
|
NP_001121362.1:p.Gln178Ter
|
|
NM_016630.6:c.613C>T
|
NP_057714.1:p.Gln205Ter
|
|
ENST00000204566.6:c.613C>T
|
ENSP00000204566.2:p.Gln205Ter
|
|
ENST00000416889.6:c.532C>T
|
ENSP00000394846.2:p.Gln178Ter
|
|
ENST00000433215.6:c.613C>T
|
ENSP00000404111.2:p.Gln205Ter
|
|
ENST00000559199.5:c.151C>T
|
ENSP00000456365.1:p.Gln51Ter
|
|
ENST00000561078.5:c.*77C>T
|
ENSP00000452865.1:n.*77C>T
|
|
XM_005254436.3:c.613C>T
|
XP_005254493.1:p.Gln205Ter
|
|
XM_005254437.3:c.613C>T
|
XP_005254494.1:p.Gln205Ter
|
|
XM_005254437.4:c.613C>T
|
XP_005254494.1:p.Gln205Ter
|
|
XM_006720564.2:c.613C>T
|
XP_006720627.1:p.Gln205Ter
|
|
XM_011521662.1:c.613C>T
|
XP_011519964.1:p.Gln205Ter
|
|
XM_017022297.1:c.613C>T
|
XP_016877786.1:p.Gln205Ter
|
|
XM_017022298.1:c.613C>T
|
XP_016877787.1:p.Gln205Ter
|