ENST00000378802.5:c.1186C>G
MANE Select
|
ENSP00000368079.4:p.Pro396Ala
|
|
ENST00000378802.4:c.1186C>G
|
ENSP00000368079.4:p.Pro396Ala
|
|
ENST00000502665.1:n.421C>G
|
|
|
ENST00000507209.5:n.5884C>G
|
|
|
ENST00000513354.5:n.276C>G
|
|
|
NM_207352.3:c.1186C>G
|
NP_997235.3:p.Pro396Ala
|
|
XM_005262935.2:c.1186C>G
|
XP_005262992.1:p.Pro396Ala
|
|
XM_006714184.2:c.790C>G
|
XP_006714247.1:p.Pro264Ala
|
|
XM_005262935.4:c.1186C>G
|
XP_005262992.1:p.Pro396Ala
|
|
XM_017008037.1:c.790C>G
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XP_016863526.1:p.Pro264Ala
|
|
NM_207352.4:c.1186C>G
MANE Select
|
NP_997235.3:p.Pro396Ala
|
|