ENST00000704337.1:n.361C>G
|
|
|
ENST00000378536.5:c.1193C>G
MANE Select
|
ENSP00000367797.4:p.Pro398Arg
|
|
ENST00000378536.4:c.1193C>G
|
ENSP00000367797.4:p.Pro398Arg
|
|
NM_003036.3:c.1193C>G
|
NP_003027.1:p.Pro398Arg
|
|
XM_005244775.2:c.1193C>G
|
XP_005244832.1:p.Pro398Arg
|
|
XM_005244776.3:c.323C>G
|
XP_005244833.1:p.Pro108Arg
|
|
XM_005244775.3:c.1193C>G
|
XP_005244832.1:p.Pro398Arg
|
|
XM_005244776.4:c.323C>G
|
XP_005244833.1:p.Pro108Arg
|
|
XM_017002128.1:c.701C>G
|
XP_016857617.1:p.Pro234Arg
|
|
NM_003036.4:c.1193C>G
MANE Select
|
NP_003027.1:p.Pro398Arg
|
|