NM_021075.4:c.11C>G
MANE Select
|
NP_066553.3:p.Pro4Arg
|
ENST00000354250.7:c.11C>G
MANE Select
|
ENSP00000346196.2:p.Pro4Arg
|
NM_001001503.1:c.11C>G
|
NP_001001503.1:p.Pro4Arg
|
NM_001001503.2:c.11C>G
|
NP_001001503.1:p.Pro4Arg
|
NM_021075.3:c.11C>G
|
NP_066553.3:p.Pro4Arg
|
ENST00000340344.4:c.11C>G
|
ENSP00000342895.3:p.Pro4Arg
|
ENST00000354250.6:c.11C>G
|
ENSP00000346196.2:p.Pro4Arg
|
ENST00000460259.1:n.572-3583C>G
|
|
ENST00000460740.1:n.24C>G
|
|
XM_011529586.1:c.11C>G
|
XP_011527888.1:p.Pro4Arg
|
XM_011529586.2:c.11C>G
|
XP_011527888.1:p.Pro4Arg
|
XM_017028359.1:c.11C>G
|
XP_016883848.1:p.Pro4Arg
|