ENST00000267845.8:c.1796C>A
MANE Select
|
ENSP00000267845.3:p.Pro599His
|
|
ENST00000267845.7:c.1796C>A
|
ENSP00000267845.3:p.Pro599His
|
|
ENST00000543581.5:c.1697C>A
|
ENSP00000440252.1:p.Pro566His
|
|
ENST00000559816.1:n.1540C>A
|
|
|
NM_001306146.1:c.1697C>A
|
NP_001293075.1:p.Pro566His
|
|
NM_002112.3:c.1796C>A
|
NP_002103.2:p.Pro599His
|
|
XM_011521479.1:c.1559C>A
|
XP_011519781.1:p.Pro520His
|
|
XM_011521480.1:c.1364C>A
|
XP_011519782.1:p.Pro455His
|
|
XM_017022094.1:c.1901C>A
|
XP_016877583.1:p.Pro634His
|
|
XM_017022095.1:c.1802C>A
|
XP_016877584.1:p.Pro601His
|
|
XM_017022096.1:c.1673C>A
|
XP_016877585.1:p.Pro558His
|
|
XM_017022097.1:c.1664C>A
|
XP_016877586.1:p.Pro555His
|
|
XM_017022098.1:c.1469C>A
|
XP_016877587.1:p.Pro490His
|
|
NM_002112.4:c.1796C>A
MANE Select
|
NP_002103.2:p.Pro599His
|
|
NM_001306146.2:c.1697C>A
|
NP_001293075.1:p.Pro566His
|
|