ENST00000229332.12:c.*236A>G
(CLEC4A)
MANE Select
|
ENSP00000229332.5:n.*236A>G
|
|
ENST00000345999.9:c.*236A>G
(CLEC4A)
|
ENSP00000344646.3:n.*236A>G
|
|
ENST00000402465.8:c.114+270A>G
|
|
|
ENST00000229332.9:c.*236A>G
(CLEC4A)
|
ENSP00000229332.5:n.*236A>G
|
|
ENST00000345999.7:c.*236A>G
(CLEC4A)
|
ENSP00000344646.3:n.*236A>G
|
|
ENST00000402465.7:c.-151+270A>G
(ZNF705A)
|
ENSP00000384896.3:n.-151+270A>G
|
|
NM_016184.3:c.*236A>G
(CLEC4A)
|
NP_057268.1:n.*236A>G
|
|
NM_194447.2:c.*236A>G
(CLEC4A)
|
NP_919429.2:n.*236A>G
|
|
NM_194448.2:c.*236A>G
(CLEC4A)
|
NP_919430.1:n.*236A>G
|
|
NM_194450.2:c.*236A>G
(CLEC4A)
|
NP_919432.1:n.*236A>G
|
|
XM_011520684.1:c.*236A>G
(CLEC4A)
|
XP_011518986.1:n.*236A>G
|
|
XM_011520684.2:c.*236A>G
(CLEC4A)
|
XP_011518986.1:n.*236A>G
|
|
XM_017019382.2:c.*236A>G
(CLEC4A)
|
XP_016874871.1:n.*236A>G
|
|
XM_024448997.1:c.*236A>G
(CLEC4A)
|
XP_024304765.1:n.*236A>G
|
|
NM_016184.4:c.*236A>G
(CLEC4A)
MANE Select
|
NP_057268.1:n.*236A>G
|
|
NM_194447.3:c.*236A>G
(CLEC4A)
|
NP_919429.2:n.*236A>G
|
|
NM_194448.3:c.*236A>G
(CLEC4A)
|
NP_919430.1:n.*236A>G
|
|
NM_194450.3:c.*236A>G
(CLEC4A)
|
NP_919432.1:n.*236A>G
|
|