|
NM_005327.7:c.881A>G
MANE Select
|
NP_005318.6:p.Asn294Ser
|
|
ENST00000309522.8:c.881A>G
MANE Select
|
ENSP00000312288.4:p.Asn294Ser
|
|
NM_001184705.2:c.932A>G
|
NP_001171634.2:p.Asn311Ser
|
|
NM_001184705.3:c.932A>G
|
NP_001171634.2:p.Asn311Ser
|
|
NM_001184705.4:c.932A>G
|
NP_001171634.3:p.Asn311Ser
|
|
NM_001331027.1:c.893A>G
|
NP_001317956.1:p.Asn298Ser
|
|
NM_001331027.2:c.893A>G
|
NP_001317956.2:p.Asn298Ser
|
|
NM_005327.4:c.881A>G
|
NP_005318.3:p.Asn294Ser
|
|
ENST00000309522.7:c.881A>G
|
ENSP00000312288.3:p.Asn294Ser
|
|
ENST00000403312.5:c.1109A>G
|
ENSP00000385638.2:p.Asn370Ser
|
|
ENST00000403312.6:c.890A>G
|
ENSP00000385638.3:p.Asn297Ser
|
|
ENST00000505878.3:c.893A>G
|
ENSP00000425952.1:p.Asn298Ser
|
|
ENST00000505878.4:c.1109A>G
|
ENSP00000425952.2:p.Asn370Ser
|
|
ENST00000507260.3:n.5400A>G
|
|
|
ENST00000510728.5:n.552A>G
|
|
|
ENST00000510728.6:n.2000A>G
|
|
|
ENST00000514776.1:n.348A>G
|
|
|
ENST00000514776.2:n.5729A>G
|
|
|
ENST00000514776.3:n.5729A>G
|
|
|
ENST00000515462.5:n.527A>G
|
|
|
ENST00000515462.6:n.2377A>G
|
|
|
ENST00000515462.7:n.2377A>G
|
|
|
ENST00000603302.5:c.932A>G
|
ENSP00000474560.1:p.Asn311Ser
|
|
ENST00000626637.1:c.893A>G
|
ENSP00000486771.1:p.Asn298Ser
|
|
ENST00000626637.2:c.893A>G
|
ENSP00000486771.1:p.Asn298Ser
|
|
ENST00000638559.1:c.739A>G
|
|
|
ENST00000638621.1:c.467A>G
|
ENSP00000491581.1:p.Asn156Ser
|
|
ENST00000638648.1:n.1032A>G
|
|
|
ENST00000638648.2:c.*274A>G
|
ENSP00000507949.1:n.*274A>G
|
|
ENST00000639146.1:c.*274A>G
|
ENSP00000492345.1:n.*274A>G
|
|
ENST00000639335.1:c.*316A>G
|
ENSP00000491310.1:n.*316A>G
|
|
ENST00000639698.1:c.688A>G
|
ENSP00000492420.1:n.688A>G
|
|
ENST00000639784.1:c.545A>G
|
|
|
ENST00000640048.1:c.853A>G
|
ENSP00000492009.1:n.853A>G
|
|
ENST00000640060.1:c.*976A>G
|
ENSP00000492734.1:n.*976A>G
|
|
ENST00000640201.1:n.1145A>G
|
|
|
ENST00000640201.2:n.1276A>G
|
|
|
ENST00000640752.1:n.5084A>G
|
|
|
ENST00000640752.2:n.5091A>G
|
|
|
ENST00000682067.1:c.660-302A>G
|
|
|
ENST00000682086.1:n.1259A>G
|
|
|
ENST00000682373.1:c.540A>G
|
|
|
ENST00000684696.1:c.*201A>G
|
ENSP00000507675.1:n.*201A>G
|
|
XM_005262972.1:c.893A>G
|
XP_005263029.1:p.Asn298Ser
|
|
XR_001741214.2:n.1106A>G
|
|
|
XR_002959727.1:n.1284A>G
|
|
|
XR_938726.1:n.1339A>G
|
|
