ENST00000704099.1:c.11881G>C
|
ENSP00000515693.1:p.Glu3961Gln
|
|
ENST00000262854.11:c.12097G>C
MANE Select
|
ENSP00000262854.6:p.Glu4033Gln
|
|
ENST00000262854.10:c.12097G>C
|
ENSP00000262854.6:p.Glu4033Gln
|
|
ENST00000342160.7:c.12097G>C
|
ENSP00000340648.3:p.Glu4033Gln
|
|
ENST00000426907.5:c.2564G>C
|
|
|
ENST00000480438.1:n.232G>C
|
|
|
ENST00000612484.4:c.12070G>C
|
ENSP00000479451.1:p.Glu4024Gln
|
|
NM_031407.6:c.12097G>C
|
NP_113584.3:p.Glu4033Gln
|
|
XM_005261965.2:c.12097G>C
|
XP_005262022.1:p.Glu4033Gln
|
|
XM_011530746.1:c.12346G>C
|
XP_011529048.1:p.Glu4116Gln
|
|
XM_011530747.1:c.12346G>C
|
XP_011529049.1:p.Glu4116Gln
|
|
XM_011530748.1:c.12346G>C
|
XP_011529050.1:p.Glu4116Gln
|
|
XM_011530749.1:c.12346G>C
|
XP_011529051.1:p.Glu4116Gln
|
|
XM_011530750.1:c.12346G>C
|
XP_011529052.1:p.Glu4116Gln
|
|
XM_011530751.1:c.12346G>C
|
XP_011529053.1:p.Glu4116Gln
|
|
XM_011530752.1:c.12343G>C
|
XP_011529054.1:p.Glu4115Gln
|
|
XM_011530753.1:c.12301G>C
|
XP_011529055.1:p.Glu4101Gln
|
|
XM_011530754.1:c.12298G>C
|
XP_011529056.1:p.Glu4100Gln
|
|
XM_011530755.1:c.12295G>C
|
XP_011529057.1:p.Glu4099Gln
|
|
XM_011530756.1:c.12247G>C
|
XP_011529058.1:p.Glu4083Gln
|
|
XM_011530757.1:c.11944G>C
|
XP_011529059.1:p.Glu3982Gln
|
|
XM_005261965.4:c.12097G>C
|
XP_005262022.1:p.Glu4033Gln
|
|
XM_011530751.2:c.12346G>C
|
XP_011529053.1:p.Glu4116Gln
|
|
XM_017029191.1:c.12478G>C
|
XP_016884680.1:p.Glu4160Gln
|
|
XM_017029192.1:c.12475G>C
|
XP_016884681.1:p.Glu4159Gln
|
|
XM_017029193.1:c.12457G>C
|
XP_016884682.1:p.Glu4153Gln
|
|
XM_017029194.1:c.12433G>C
|
XP_016884683.1:p.Glu4145Gln
|
|
XM_017029195.1:c.12430G>C
|
XP_016884684.1:p.Glu4144Gln
|
|
XM_017029196.1:c.12427G>C
|
XP_016884685.1:p.Glu4143Gln
|
|
XM_017029197.1:c.12379G>C
|
XP_016884686.1:p.Glu4127Gln
|
|
XM_017029198.2:c.12367G>C
|
XP_016884687.1:p.Glu4123Gln
|
|
XM_017029199.1:c.12367G>C
|
XP_016884688.1:p.Glu4123Gln
|
|
XM_017029200.1:c.12367G>C
|
XP_016884689.1:p.Glu4123Gln
|
|
XM_017029201.1:c.12367G>C
|
XP_016884690.1:p.Glu4123Gln
|
|
XM_017029202.1:c.12367G>C
|
XP_016884691.1:p.Glu4123Gln
|
|
XM_017029203.1:c.12367G>C
|
XP_016884692.1:p.Glu4123Gln
|
|
XM_017029204.1:c.12229G>C
|
XP_016884693.1:p.Glu4077Gln
|
|
XM_017029206.1:c.12076G>C
|
XP_016884695.1:p.Glu4026Gln
|
|
XM_024452322.1:c.12346G>C
|
XP_024308090.1:p.Glu4116Gln
|
|
NM_031407.7:c.12097G>C
MANE Select
|
NP_113584.3:p.Glu4033Gln
|
|