ENST00000309383.6:c.2092C>G
MANE Select
|
ENSP00000310649.1:p.Pro698Ala
|
|
ENST00000309383.5:c.2092C>G
|
ENSP00000310649.1:p.Pro698Ala
|
|
ENST00000326848.7:c.1177C>G
|
ENSP00000320853.7:p.Pro393Ala
|
|
ENST00000590333.5:c.2140C>G
|
ENSP00000468190.1:p.Pro714Ala
|
|
NM_032430.1:c.2092C>G
|
NP_115806.1:p.Pro698Ala
|
|
XM_005259327.2:c.1822C>G
|
XP_005259384.1:p.Pro608Ala
|
|
XM_011527395.1:c.1849C>G
|
XP_011525697.1:p.Pro617Ala
|
|
XR_430213.2:n.2075C>G
|
|
|
XM_005259327.3:c.1822C>G
|
XP_005259384.1:p.Pro608Ala
|
|
XM_011527395.2:c.1564C>G
|
XP_011525697.2:p.Pro522Ala
|
|
XM_024451739.1:c.1867C>G
|
XP_024307507.1:p.Pro623Ala
|
|
XR_430213.4:n.2373C>G
|
|
|
NM_032430.2:c.2092C>G
MANE Select
|
NP_115806.1:p.Pro698Ala
|
|