ENST00000460680.6:c.2111T>G
MANE Select
|
ENSP00000417132.1:p.Val704Gly
|
|
ENST00000296288.9:c.2057T>G
|
ENSP00000296288.5:p.Val686Gly
|
|
ENST00000460680.5:c.2111T>G
|
ENSP00000417132.1:p.Val704Gly
|
|
ENST00000466093.1:n.784T>G
|
|
|
ENST00000469613.5:c.310T>G
|
|
|
ENST00000478368.1:c.683T>G
|
ENSP00000420647.1:p.Val228Gly
|
|
NM_004656.3:c.2111T>G
|
NP_004647.1:p.Val704Gly
|
|
XM_011534149.1:c.2180T>G
|
XP_011532451.1:p.Val727Gly
|
|
XM_011534150.1:c.2135T>G
|
XP_011532452.1:p.Val712Gly
|
|
XM_011534151.1:c.2126T>G
|
XP_011532453.1:p.Val709Gly
|
|
XM_011534152.1:c.2066T>G
|
XP_011532454.1:p.Val689Gly
|
|
XM_011534149.3:c.2180T>G
|
XP_011532451.1:p.Val727Gly
|
|
XM_011534150.3:c.2135T>G
|
XP_011532452.1:p.Val712Gly
|
|
XM_011534151.3:c.2126T>G
|
XP_011532453.1:p.Val709Gly
|
|
XM_011534152.2:c.2066T>G
|
XP_011532454.1:p.Val689Gly
|
|
XM_017007303.2:c.2057T>G
|
XP_016862792.1:p.Val686Gly
|
|
NM_004656.4:c.2111T>G
MANE Select
|
NP_004647.1:p.Val704Gly
|
|