ENST00000399503.4:c.2630T>G
MANE Select
|
ENSP00000382423.3:p.Leu877Trp
|
|
ENST00000399503.3:c.2630T>G
|
ENSP00000382423.3:p.Leu877Trp
|
|
NM_005921.1:c.2630T>G
|
NP_005912.1:p.Leu877Trp
|
|
XM_005248519.3:c.2252T>G
|
XP_005248576.2:p.Leu751Trp
|
|
XM_011543406.1:c.2375T>G
|
XP_011541708.1:p.Leu792Trp
|
|
XM_011543407.1:c.2351T>G
|
XP_011541709.1:p.Leu784Trp
|
|
XM_011543408.1:c.2630T>G
|
XP_011541710.1:p.Leu877Trp
|
|
XM_017009484.1:c.2219T>G
|
XP_016864973.1:p.Leu740Trp
|
|
XM_017009485.1:c.2141T>G
|
XP_016864974.1:p.Leu714Trp
|
|
XR_001742068.2:n.2661T>G
|
|
|
NM_005921.2:c.2630T>G
MANE Select
|
NP_005912.1:p.Leu877Trp
|
|