|
NM_015668.5:c.2154C>G
MANE Select
|
NP_056483.3:p.Cys718Trp
|
|
ENST00000360863.11:c.2154C>G
MANE Select
|
ENSP00000354109.6:p.Cys718Trp
|
|
NM_001286692.1:c.2118C>G
|
NP_001273621.1:p.Cys706Trp
|
|
NM_001286692.2:c.2118C>G
|
NP_001273621.1:p.Cys706Trp
|
|
NM_001286693.1:c.1611C>G
|
NP_001273622.1:p.Cys537Trp
|
|
NM_001286693.2:c.1611C>G
|
NP_001273622.1:p.Cys537Trp
|
|
NM_015668.4:c.2154C>G
|
NP_056483.3:p.Cys718Trp
|
|
ENST00000360863.10:c.2154C>G
|
ENSP00000354109.6:p.Cys718Trp
|
|
ENST00000517769.5:n.382C>G
|
|
|
ENST00000517828.5:c.112-30374C>G
|
ENSP00000427754.1:n.112-30374C>G
|
|
ENST00000518474.1:n.389C>G
|
|
|
ENST00000519725.5:c.*729C>G
|
ENSP00000427798.1:n.*729C>G
|
|
ENST00000520923.5:n.1956C>G
|
|
|
ENST00000523287.5:c.1611C>G
|
ENSP00000429382.1:p.Cys537Trp
|
|
ENST00000523437.5:c.2118C>G
|
ENSP00000428212.1:p.Cys706Trp
|
|
ENST00000617334.1:c.2118C>G
|
ENSP00000479205.1:p.Cys706Trp
|
|
XM_005250856.2:c.2154C>G
|
XP_005250913.1:p.Cys718Trp
|
|
XM_005250856.3:c.2154C>G
|
XP_005250913.1:p.Cys718Trp
|
|
XM_005250857.2:c.2154C>G
|
XP_005250914.1:p.Cys718Trp
|
|
XM_005250857.3:c.2154C>G
|
XP_005250914.1:p.Cys718Trp
|
|
XM_005250858.2:c.2154C>G
|
XP_005250915.1:p.Cys718Trp
|
|
XM_005250858.3:c.2154C>G
|
XP_005250915.1:p.Cys718Trp
|
|
XM_005250860.2:c.2154C>G
|
XP_005250917.1:p.Cys718Trp
|
|
XM_005250860.3:c.2154C>G
|
XP_005250917.1:p.Cys718Trp
|
|
XM_006716540.2:c.1866C>G
|
XP_006716603.1:p.Cys622Trp
|
|
XM_011516957.1:c.1866C>G
|
XP_011515259.1:p.Cys622Trp
|
|
XM_011516958.1:c.1866C>G
|
XP_011515260.1:p.Cys622Trp
|
|
XM_011516959.1:c.2154C>G
|
XP_011515261.1:p.Cys718Trp
|
|
XM_011516959.3:c.2154C>G
|
XP_011515261.1:p.Cys718Trp
|
|
XM_017013309.2:c.2154C>G
|
XP_016868798.1:p.Cys718Trp
|
|
XM_017013310.2:c.2154C>G
|
XP_016868799.1:p.Cys718Trp
|
|
XM_017013311.1:c.789C>G
|
XP_016868800.1:p.Cys263Trp
|
|
XM_024447121.1:c.321C>G
|
XP_024302889.1:p.Cys107Trp
|
|
XM_024447122.1:c.321C>G
|
XP_024302890.1:p.Cys107Trp
|
|
XR_928317.1:n.1864+8520C>G
|
|
