|
ENST00000379608.9:c.620C>G
(TFAP2A)
|
ENSP00000368928.3:p.Ser207Ter
|
|
|
ENST00000379613.10:c.644C>G
(TFAP2A)
MANE Select
|
ENSP00000368933.5:p.Ser215Ter
|
|
|
ENST00000482890.6:c.644C>G
(TFAP2A)
|
ENSP00000418541.2:p.Ser215Ter
|
|
|
ENST00000488193.7:c.*135C>G
(TFAP2A)
|
ENSP00000419823.3:n.*135C>G
|
|
|
ENST00000498450.3:c.209C>G
(TFAP2A)
|
ENSP00000419961.3:p.Ser70Ter
|
|
|
ENST00000319516.8:c.626C>G
(TFAP2A)
|
ENSP00000316516.4:p.Ser209Ter
|
|
|
ENST00000379608.7:c.620C>G
(TFAP2A)
|
ENSP00000368928.3:p.Ser207Ter
|
|
|
ENST00000379613.7:c.644C>G
(TFAP2A)
|
ENSP00000368933.3:p.Ser215Ter
|
|
|
ENST00000466073.5:c.638C>G
(TFAP2A)
|
ENSP00000417495.1:p.Ser213Ter
|
|
|
ENST00000475264.5:c.352C>G
(TFAP2A)
|
|
|
|
ENST00000478375.5:n.638C>G
(TFAP2A)
|
|
|
|
ENST00000482890.5:c.638C>G
(TFAP2A)
|
ENSP00000418541.1:p.Ser213Ter
|
|
|
ENST00000488193.5:c.*135C>G
(TFAP2A)
|
ENSP00000419823.1:n.*135C>G
|
|
|
ENST00000489805.5:c.*135C>G
(TFAP2A)
|
ENSP00000420568.1:n.*135C>G
|
|
|
ENST00000490875.5:n.880C>G
(TFAP2A)
|
|
|
|
ENST00000497266.5:n.609C>G
(TFAP2A)
|
|
|
|
ENST00000498450.1:c.209C>G
(TFAP2A)
|
ENSP00000419961.1:p.Ser70Ter
|
|
|
NM_001032280.2:c.620C>G
(TFAP2A)
|
NP_001027451.1:p.Ser207Ter
|
|
|
NM_001042425.1:c.626C>G
(TFAP2A)
|
NP_001035890.1:p.Ser209Ter
|
|
|
NM_003220.2:c.638C>G
(TFAP2A)
|
NP_003211.1:p.Ser213Ter
|
|
|
XM_006715175.2:c.773C>G
(TFAP2A)
|
XP_006715238.1:p.Ser258Ter
|
|
|
XM_011514833.1:c.488C>G
(TFAP2A)
|
XP_011513135.1:p.Ser163Ter
|
|
|
NR_145448.1:n.133G>C
(TFAP2A-AS2)
|
|
|
|
XM_011514833.2:c.488C>G
(TFAP2A)
|
XP_011513135.1:p.Ser163Ter
|
|
|
XM_017011232.1:c.884C>G
(TFAP2A)
|
XP_016866721.1:p.Ser295Ter
|
|
|
NM_003220.3:c.638C>G
(TFAP2A)
|
NP_003211.1:p.Ser213Ter
|
|
|
NM_001032280.3:c.620C>G
(TFAP2A)
|
NP_001027451.1:p.Ser207Ter
|
|
|
NM_001042425.2:c.626C>G
(TFAP2A)
|
NP_001035890.1:p.Ser209Ter
|
|
|
NM_001372066.1:c.644C>G
(TFAP2A)
MANE Select
|
NP_001358995.1:p.Ser215Ter
|
|
|
NM_001042425.3:c.626C>G
(TFAP2A)
|
NP_001035890.1:p.Ser209Ter
|
|
