ENST00000237596.7:c.1357C>G
MANE Select
|
ENSP00000237596.2:p.Pro453Ala
|
|
ENST00000237596.6:c.1357C>G
|
ENSP00000237596.2:p.Pro453Ala
|
|
ENST00000508588.5:c.-199+3222C>G
|
ENSP00000427131.1:n.-199+3222C>G
|
|
NM_000297.3:c.1357C>G
|
NP_000288.1:p.Pro453Ala
|
|
XM_011532028.1:c.1132C>G
|
XP_011530330.1:p.Pro378Ala
|
|
XM_011532029.1:c.637C>G
|
XP_011530331.1:p.Pro213Ala
|
|
XM_011532030.1:c.517C>G
|
XP_011530332.1:p.Pro173Ala
|
|
XR_244632.2:n.1452C>G
|
|
|
NR_156488.1:n.1444C>G
|
|
|
XM_011532028.2:c.1132C>G
|
XP_011530330.1:p.Pro378Ala
|
|
XM_011532030.2:c.517C>G
|
XP_011530332.1:p.Pro173Ala
|
|
NM_000297.4:c.1357C>G
MANE Select
|
NP_000288.1:p.Pro453Ala
|
|
NR_156488.2:n.1456C>G
|
|
|