ENST00000466617.6:c.2405_2411delinsTCAAGGG
|
ENSP00000420082.2:p.Val802=
|
|
ENST00000470367.2:c.2693_2699delinsTCAAGGG
|
ENSP00000514541.1:p.Val898=
|
|
ENST00000483566.2:c.2405_2411delinsTCAAGGG
|
ENSP00000420252.2:p.Val802=
|
|
ENST00000699714.1:c.2405_2411delinsTCAAGGG
|
ENSP00000514539.1:p.Val802=
|
|
ENST00000699715.1:c.2405_2411delinsTCAAGGG
|
ENSP00000514540.1:p.Val802=
|
|
ENST00000699716.1:c.2405_2411delinsTCAAGGG
|
ENSP00000514542.1:p.Val802=
|
|
ENST00000699717.1:n.2131_2137delinsTCAAGGG
|
|
|
ENST00000699718.1:c.3803_3809delinsTCAAGGG
|
ENSP00000514543.1:p.Val1268=
|
|
ENST00000462833.6:c.3728_3734delinsTCAAGGG
MANE Select
|
ENSP00000419361.1:p.Val1243=
|
|
ENST00000309879.9:c.2678_2684delinsTCAAGGG
|
ENSP00000308685.5:p.Val893=
|
|
ENST00000462833.5:c.3728_3734delinsTCAAGGG
|
ENSP00000419361.1:p.Val1243=
|
|
ENST00000478092.1:n.498_504delinsTCAAGGG
|
|
|
ENST00000491190.5:c.2702_2708delinsTCAAGGG
|
ENSP00000418537.1:p.Val901=
|
|
NM_001199642.1:c.2678_2684delinsTCAAGGG
|
NP_001186571.1:p.Val893=
|
|
NM_183357.2:c.3728_3734delinsTCAAGGG
|
NP_899200.1:p.Val1243=
|
|
XM_005247077.2:c.3803_3809delinsTCAAGGG
|
XP_005247134.1:p.Val1268=
|
|
XM_005247078.1:c.2753_2759delinsTCAAGGG
|
XP_005247135.1:p.Val918=
|
|
XM_006713483.1:c.2702_2708delinsTCAAGGG
|
XP_006713546.1:p.Val901=
|
|
XM_006713484.1:c.2480_2486delinsTCAAGGG
|
XP_006713547.1:p.Val827=
|
|
XM_011512359.1:c.2804_2810delinsTCAAGGG
|
XP_011510661.1:p.Val935=
|
|
XM_011512360.1:c.2714_2720delinsTCAAGGG
|
XP_011510662.1:p.Val905=
|
|
XM_011512361.1:c.2480_2486delinsTCAAGGG
|
XP_011510663.1:p.Val827=
|
|
XM_005247077.4:c.3803_3809delinsTCAAGGG
|
XP_005247134.1:p.Val1268=
|
|
XM_011512359.2:c.2804_2810delinsTCAAGGG
|
XP_011510661.1:p.Val935=
|
|
XM_011512360.3:c.2714_2720delinsTCAAGGG
|
XP_011510662.1:p.Val905=
|
|
XM_017005638.1:c.2705_2711delinsTCAAGGG
|
XP_016861127.1:p.Val902=
|
|
XM_017005639.1:c.2705_2711delinsTCAAGGG
|
XP_016861128.1:p.Val902=
|
|
NM_001378259.1:c.3803_3809delinsTCAAGGG
|
NP_001365188.1:p.Val1268=
|
|
NM_183357.3:c.3728_3734delinsTCAAGGG
MANE Select
|
NP_899200.1:p.Val1243=
|
|