|
NM_004006.3:c.8996C>T
MANE Select
|
NP_003997.2:p.Ala2999Val
|
|
ENST00000357033.9:c.8996C>T
MANE Select
|
ENSP00000354923.3:p.Ala2999Val
|
|
NM_000109.3:c.8972C>T
|
NP_000100.2:p.Ala2991Val
|
|
NM_000109.4:c.8972C>T
|
NP_000100.3:p.Ala2991Val
|
|
NM_004006.2:c.8996C>T , LRG_199t1:c.8996C>T
|
NP_003997.1:p.Ala2999Val
|
|
NM_004009.3:c.8984C>T
|
NP_004000.1:p.Ala2995Val
|
|
NM_004010.3:c.8627C>T
|
NP_004001.1:p.Ala2876Val
|
|
NM_004011.3:c.4973C>T
|
NP_004002.2:p.Ala1658Val
|
|
NM_004011.4:c.4973C>T
|
NP_004002.3:p.Ala1658Val
|
|
NM_004012.3:c.4964C>T
|
NP_004003.1:p.Ala1655Val
|
|
NM_004012.4:c.4964C>T
|
NP_004003.2:p.Ala1655Val
|
|
NM_004013.2:c.1616C>T
|
NP_004004.1:p.Ala539Val
|
|
NM_004013.3:c.1616C>T
|
NP_004004.2:p.Ala539Val
|
|
NM_004014.2:c.809C>T
|
NP_004005.1:p.Ala270Val
|
|
NM_004014.3:c.809C>T
|
NP_004005.2:p.Ala270Val
|
|
NM_004020.3:c.1616C>T
|
NP_004011.2:p.Ala539Val
|
|
NM_004020.4:c.1616C>T
|
NP_004011.3:p.Ala539Val
|
|
NM_004021.2:c.1616C>T
|
NP_004012.1:p.Ala539Val
|
|
NM_004021.3:c.1616C>T
|
NP_004012.2:p.Ala539Val
|
|
NM_004022.2:c.1616C>T
|
NP_004013.1:p.Ala539Val
|
|
NM_004022.3:c.1616C>T
|
NP_004013.2:p.Ala539Val
|
|
NM_004023.2:c.1616C>T
|
NP_004014.1:p.Ala539Val
|
|
NM_004023.3:c.1616C>T
|
NP_004014.2:p.Ala539Val
|
|
ENST00000343523.6:c.809C>T
|
ENSP00000340057.3:p.Ala270Val
|
|
ENST00000343523.7:c.851C>T
|
ENSP00000340057.4:p.Ala284Val
|
|
ENST00000357033.8:c.8996C>T
|
ENSP00000354923.3:p.Ala2999Val
|
|
ENST00000358062.6:c.2084C>T
|
ENSP00000350765.2:p.Ala695Val
|
|
ENST00000358062.7:c.3842C>T
|
ENSP00000350765.3:p.Ala1281Val
|
|
ENST00000359836.5:c.1616C>T
|
ENSP00000352894.1:p.Ala539Val
|
|
ENST00000378677.6:c.8984C>T
|
ENSP00000367948.2:p.Ala2995Val
|
|
ENST00000378707.7:c.1616C>T
|
ENSP00000367979.3:p.Ala539Val
|
|
ENST00000474231.5:c.1616C>T
|
ENSP00000417123.1:p.Ala539Val
|
|
ENST00000541735.5:c.1616C>T
|
ENSP00000444119.1:p.Ala539Val
|
|
ENST00000619831.4:c.8981C>T
|
ENSP00000479270.1:p.Ala2994Val
|
|
ENST00000619831.5:c.4964C>T
|
ENSP00000479270.2:p.Ala1655Val
|
|
ENST00000620040.4:c.8993C>T
|
ENSP00000478150.1:p.Ala2998Val
|
|
ENST00000620040.5:c.1616C>T
|
ENSP00000478150.2:p.Ala539Val
|
|
ENST00000680961.1:c.1616C>T
|
ENSP00000506386.1:p.Ala539Val
|
|
ENST00000681646.1:n.2657C>T
|
|
|
ENST00000682238.1:c.1616C>T
|
ENSP00000508124.1:p.Ala539Val
|
|
ENST00000683450.1:n.2461C>T
|
|
|
ENST00000683957.1:n.2488C>T
|
|
|
ENST00000684130.1:c.1616C>T
|
ENSP00000508037.1:p.Ala539Val
|
|
XM_006724468.2:c.8996C>T
|
XP_006724531.1:p.Ala2999Val
|
|
XM_006724469.2:c.8972C>T
|
XP_006724532.1:p.Ala2991Val
|
|
XM_006724469.3:c.8972C>T
|
XP_006724532.1:p.Ala2991Val
|
|
XM_006724470.2:c.8996C>T
|
XP_006724533.1:p.Ala2999Val
|
|
XM_006724470.3:c.8996C>T
|
XP_006724533.1:p.Ala2999Val
|
|
XM_006724471.2:c.8996C>T
|
XP_006724534.1:p.Ala2999Val
|
|
XM_006724472.2:c.8867C>T
|
XP_006724535.1:p.Ala2956Val
|
|
XM_006724473.2:c.8858C>T
|
XP_006724536.1:p.Ala2953Val
|
|
XM_006724474.2:c.8996C>T
|
XP_006724537.1:p.Ala2999Val
|
|
XM_006724474.3:c.8996C>T
|
XP_006724537.1:p.Ala2999Val
|
|
XM_006724475.2:c.8996C>T
|
XP_006724538.1:p.Ala2999Val
|
|
XM_011545467.1:c.8873C>T
|
XP_011543769.1:p.Ala2958Val
|
|
XM_011545468.1:c.8996C>T
|
XP_011543770.1:p.Ala2999Val
|
|
XM_011545468.2:c.8996C>T
|
XP_011543770.1:p.Ala2999Val
|
|
XM_017029328.1:c.8996C>T
|
XP_016884817.1:p.Ala2999Val
|
|
XM_017029331.1:c.3170C>T
|
XP_016884820.1:p.Ala1057Val
|
