ENST00000318471.5:c.897C>T
MANE Select
|
ENSP00000315680.3:p.Pro299=
|
|
ENST00000541292.6:c.*162C>T
|
ENSP00000441004.1:n.*162C>T
|
|
ENST00000678002.1:c.585C>T
|
|
|
ENST00000678557.1:c.783C>T
|
ENSP00000502962.1:p.Pro261=
|
|
ENST00000679286.1:c.777C>T
|
ENSP00000503168.1:p.Pro259=
|
|
ENST00000318471.4:c.897C>T
|
ENSP00000315680.3:p.Pro299=
|
|
NM_000288.3:c.897C>T
|
NP_000279.1:p.Pro299=
|
|
XM_005267019.3:c.783C>T
|
XP_005267076.1:p.Pro261=
|
|
XM_006715502.1:c.603C>T
|
XP_006715565.1:p.Pro201=
|
|
XM_005267019.4:c.783C>T
|
XP_005267076.1:p.Pro261=
|
|
XM_006715502.2:c.603C>T
|
XP_006715565.1:p.Pro201=
|
|
XM_017010934.2:c.*20C>T
|
XP_016866423.1:n.*20C>T
|
|
NM_000288.4:c.897C>T
MANE Select
|
NP_000279.1:p.Pro299=
|
|