|
NM_002204.4:c.2155G=
MANE Select
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NP_002195.1:p.Ala719=
|
|
ENST00000320031.13:c.2155G=
MANE Select
|
ENSP00000315190.8:p.Ala719=
|
|
NM_002204.2:c.2155G=
|
NP_002195.1:p.Ala719=
|
|
NM_002204.3:c.2155G=
|
NP_002195.1:p.Ala719=
|
|
NM_005501.2:c.2155G=
|
NP_005492.1:p.Ala719=
|
|
ENST00000007722.11:c.2155G=
|
ENSP00000007722.7:p.Ala719=
|
|
ENST00000320031.12:c.2155G=
|
ENSP00000315190.8:p.Ala719=
|
|
ENST00000505306.5:n.3076G=
|
|
|
ENST00000506827.1:c.290G=
|
|
|
ENST00000507771.5:n.64G=
|
|
|
ENST00000515147.1:n.58G=
|
|
|
XM_005257308.1:c.1750G=
|
XP_005257365.1:p.Ala584=
|
|
XM_005257308.2:c.1750G=
|
XP_005257365.1:p.Ala584=
|
|
XR_001752507.1:n.2571G=
|
|