ENST00000281928.9:c.5084C>T
MANE Select
|
ENSP00000281928.3:p.Ser1695Phe
|
|
ENST00000549786.2:c.4512C>T
|
|
|
ENST00000648379.1:n.3452C>T
|
|
|
ENST00000648737.1:n.4848C>T
|
|
|
ENST00000648825.1:n.1824C>T
|
|
|
ENST00000648916.1:n.3095C>T
|
|
|
ENST00000649146.1:n.2327C>T
|
|
|
ENST00000649607.1:c.3268C>T
|
|
|
ENST00000649775.1:c.1573C>T
|
|
|
ENST00000650226.1:c.5084C>T
|
ENSP00000496981.1:p.Ser1695Phe
|
|
ENST00000281928.7:c.5084C>T
|
ENSP00000281928.3:p.Ser1695Phe
|
|
ENST00000549786.1:c.448C>T
|
|
|
ENST00000552340.1:c.116C>T
|
ENSP00000449876.1:p.Ser39Phe
|
|
NM_015335.4:c.5084C>T
|
NP_056150.1:p.Ser1695Phe
|
|
XM_011538080.1:c.5084C>T
|
XP_011536382.1:p.Ser1695Phe
|
|
XM_011538081.1:c.5081C>T
|
XP_011536383.1:p.Ser1694Phe
|
|
XM_011538082.1:c.5054C>T
|
XP_011536384.1:p.Ser1685Phe
|
|
XM_011538080.2:c.5084C>T
|
XP_011536382.1:p.Ser1695Phe
|
|
XM_011538081.2:c.5081C>T
|
XP_011536383.1:p.Ser1694Phe
|
|
XM_011538082.2:c.5054C>T
|
XP_011536384.1:p.Ser1685Phe
|
|
XM_017019090.1:c.5081C>T
|
XP_016874579.1:p.Ser1694Phe
|
|
NM_015335.5:c.5084C>T
MANE Select
|
NP_056150.1:p.Ser1695Phe
|
|