ENST00000286657.10:c.1743C>G
MANE Select
|
ENSP00000286657.4:p.Pro581=
|
|
ENST00000286657.8:c.1743C>G
|
ENSP00000286657.4:p.Pro581=
|
|
ENST00000622135.1:c.1743C>G
|
ENSP00000480055.1:p.Pro581=
|
|
NM_014243.2:c.1743C>G
|
NP_055058.2:p.Pro581=
|
|
XM_011532421.1:c.1686C>G
|
XP_011530723.1:p.Pro562=
|
|
XM_011532422.1:c.1659C>G
|
XP_011530724.1:p.Pro553=
|
|
XM_011532423.1:c.1101C>G
|
XP_011530725.1:p.Pro367=
|
|
XM_011532424.1:c.1011C>G
|
XP_011530726.1:p.Pro337=
|
|
XM_011532421.2:c.1686C>G
|
XP_011530723.1:p.Pro562=
|
|
XM_011532422.3:c.1659C>G
|
XP_011530724.1:p.Pro553=
|
|
NM_014243.3:c.1743C>G
MANE Select
|
NP_055058.2:p.Pro581=
|
|