ENST00000256084.8:c.3035C>G
MANE Select
|
ENSP00000256084.7:p.Pro1012Arg
|
|
ENST00000256084.7:c.3035C>G
|
ENSP00000256084.7:p.Pro1012Arg
|
|
ENST00000359874.7:c.3125C>G
|
ENSP00000352936.3:p.Pro1042Arg
|
|
NM_001127698.1:c.3125C>G
|
NP_001121170.1:p.Pro1042Arg
|
|
NM_006846.3:c.3035C>G , LRG_110t1:c.3035C>G
|
NP_006837.2:p.Pro1012Arg
|
|
XM_011537550.1:c.3068C>G
|
XP_011535852.1:p.Pro1023Arg
|
|
XM_011537551.1:c.3041C>G
|
XP_011535853.1:p.Pro1014Arg
|
|
XM_011537551.2:c.3041C>G
|
XP_011535853.1:p.Pro1014Arg
|
|
NM_001127698.2:c.3125C>G
|
NP_001121170.1:p.Pro1042Arg
|
|
NM_006846.4:c.3035C>G
MANE Select
|
NP_006837.2:p.Pro1012Arg
|
|