ENST00000330889.8:c.1005A>G
MANE Select
|
ENSP00000329468.3:p.Pro335=
|
|
ENST00000330889.7:c.1005A>G
|
ENSP00000329468.3:p.Pro335=
|
|
ENST00000470962.1:n.425A>G
|
|
|
ENST00000480980.1:n.439A>G
|
|
|
ENST00000580525.5:c.1023A>G
|
ENSP00000464121.1:p.Pro341=
|
|
ENST00000581285.5:c.921A>G
|
ENSP00000464155.1:p.Pro307=
|
|
ENST00000584828.5:c.374A>G
|
|
|
ENST00000585130.5:c.*604A>G
|
ENSP00000464120.1:n.*604A>G
|
|
NM_018404.2:c.1005A>G
|
NP_060874.1:p.Pro335=
|
|
XM_005258008.2:c.1023A>G
|
XP_005258065.1:p.Pro341=
|
|
XM_005258011.2:c.960A>G
|
XP_005258068.1:p.Pro320=
|
|
XM_006721973.2:c.1023A>G
|
XP_006722036.1:p.Pro341=
|
|
XM_011524993.1:c.1020A>G
|
XP_011523295.1:p.Pro340=
|
|
XM_011524994.1:c.1002A>G
|
XP_011523296.1:p.Pro334=
|
|
NM_001346712.1:c.1023A>G
|
NP_001333641.1:p.Pro341=
|
|
NM_001346714.1:c.1002A>G
|
NP_001333643.1:p.Pro334=
|
|
NM_001346716.1:c.1005A>G
|
NP_001333645.1:p.Pro335=
|
|
NR_144488.1:n.1204A>G
|
|
|
XM_024450831.1:c.1005A>G
|
XP_024306599.1:p.Pro335=
|
|
XM_024450832.1:c.1020A>G
|
XP_024306600.1:p.Pro340=
|
|
XM_024450833.1:c.960A>G
|
XP_024306601.1:p.Pro320=
|
|
XM_024450834.1:c.1023A>G
|
XP_024306602.1:p.Pro341=
|
|
XM_024450835.1:c.639A>G
|
XP_024306603.1:p.Pro213=
|
|
NM_018404.3:c.1005A>G
MANE Select
|
NP_060874.1:p.Pro335=
|
|
NM_001346712.2:c.1023A>G
|
NP_001333641.1:p.Pro341=
|
|
NM_001346714.2:c.1002A>G
|
NP_001333643.1:p.Pro334=
|
|
NM_001346716.2:c.1005A>G
|
NP_001333645.1:p.Pro335=
|
|
NR_144488.2:n.995A>G
|
|
|