ENST00000399503.4:c.2529T>G
MANE Select
|
ENSP00000382423.3:p.Val843=
|
|
ENST00000399503.3:c.2529T>G
|
ENSP00000382423.3:p.Val843=
|
|
NM_005921.1:c.2529T>G
|
NP_005912.1:p.Val843=
|
|
XM_005248519.3:c.2151T>G
|
XP_005248576.2:p.Val717=
|
|
XM_011543406.1:c.2274T>G
|
XP_011541708.1:p.Val758=
|
|
XM_011543407.1:c.2250T>G
|
XP_011541709.1:p.Val750=
|
|
XM_011543408.1:c.2529T>G
|
XP_011541710.1:p.Val843=
|
|
XM_017009484.1:c.2118T>G
|
XP_016864973.1:p.Val706=
|
|
XM_017009485.1:c.2040T>G
|
XP_016864974.1:p.Val680=
|
|
XR_001742068.2:n.2560T>G
|
|
|
NM_005921.2:c.2529T>G
MANE Select
|
NP_005912.1:p.Val843=
|
|