ENST00000541682.7:c.526C>G
MANE Select
|
ENSP00000446205.2:p.Pro176Ala
|
|
ENST00000317814.8:c.511C>G
|
ENSP00000314774.4:p.Pro171Ala
|
|
ENST00000541682.6:c.526C>G
|
ENSP00000446205.2:p.Pro176Ala
|
|
NM_001165967.1:c.526C>G
|
NP_001159439.1:p.Pro176Ala
|
|
NM_032580.3:c.511C>G
|
NP_115969.2:p.Pro171Ala
|
|
XM_011524038.1:c.631C>G
|
XP_011522340.1:p.Pro211Ala
|
|
XM_011524039.1:c.622C>G
|
XP_011522341.1:p.Pro208Ala
|
|
XM_011524040.1:c.622C>G
|
XP_011522342.1:p.Pro208Ala
|
|
XM_011524041.1:c.613C>G
|
XP_011522343.1:p.Pro205Ala
|
|
XM_011524042.1:c.484C>G
|
XP_011522344.1:p.Pro162Ala
|
|
XR_934203.1:n.69+1924G>C
|
|
|
XM_017025232.1:c.631C>G
|
XP_016880721.1:p.Pro211Ala
|
|
XM_024451007.1:c.631C>G
|
XP_024306775.1:p.Pro211Ala
|
|
NM_001165967.2:c.526C>G
MANE Select
|
NP_001159439.1:p.Pro176Ala
|
|
NM_032580.4:c.511C>G
|
NP_115969.2:p.Pro171Ala
|
|